Site-selective amination and/or nitrilation via metal-free C(sp²)–C(sp³) cleavage of benzylic and allylic alcohols

Abstract

Benzylic/allylic alcohols are converted via site-selective C(sp²)–C(sp³) cleavage to value-added nitrogenous motifs, viz., anilines and/or nitriles as well as N-heterocycles, utilizing commercial hydroxylamine-O-sulfonic acid (HOSA) and Et₃N in an operationally simple, one-pot process. Notably, cyclic benzylic/allylic alcohols undergo bis-functionalization with attendant increases in architectural complexity and step-economy.

Benzylic/allylic alcohols are converted via site-selective C(sp²)–C(sp³) cleavage to value-added nitrogenous motifs, viz., anilines and/or nitriles as well as N-heterocycles, utilizing commercial hydroxylamine-O-sulfonic acid (HOSA) and Et₃N in an operationally simple, one-pot process.

Introduction

In recognition of increasingly strict conservational and regulatory imperatives,¹ much attention is now focused upon innovative functionalization methodologies² that are applicable to more readily available and economic feedstocks,³ while simultaneously emphasizing environmentally friendly, especially metal-free, reaction conditions.⁴ To these ends, there has been encouraging progress recently in the application of site-selective C(sp²)–C(sp³) and C(sp²)–C(sp²) cleavage strategies,⁵ despite the comparatively high bond dissociation energy of most unstrained C–C bonds and the formidable challenges posed by discriminating amongst otherwise chemically equivalent C–C bonds⁶ (Fig. 1).

Fig. 1. Representative site-selective functionalizations via C(sp²)–C(sp³) and C(sp²)–C(sp²) cleavage. ^aSelect examples of olefin α-cleavage. ^bAlkyl- and alkene-aryl cleavages. ^cC(sp²)–C(sp³) cleavages of acyclic benzyl alcohols to 1° anilines. ^dC(sp²)–C(sp³) cleavages of acyclic benzyl alcohols leading to 1° & 2° anilines. ^eThis work: C(sp²)–C(sp³) cleavage of benzylic and allylic alcohols delivering anilines and/or nitriles or N-heterocycles. FG = functional group.

Canonical syntheses of anilines⁷ and other nitrogen containing functional groups are often trammeled by multi-step sequences,⁸ harsh reaction conditions,⁹ limited scope,¹⁰ and/or lack of regioselectivity. Given the continuing interest in nitrogenous compounds,¹¹ especially anilines¹² and nitriles, by the pharmaceutical, dye, agricultural, and specialty materials markets, several novel, site-selective procedures have been introduced, intra alia, decarboxylative aminations,¹³ transition metal cross-couplings (e.g., Buchwald–Hartwig,¹⁴ Chan–Lam¹⁵), electrophilic amination reagents,¹⁶ ligand-directed aminations,¹⁷ and boronate rearrangement.¹⁸ More recently, influential examples from the Jiao^19,20 and Hashmi²¹ laboratories pioneered efficient, site-specific C–C cleavages of benzylic alcohols, alkylarenes and styrenes to anilines. Herein, we describe the operationally simple, one-pot, site-selective C(sp²)–C(sp³) cleavage of benzylic/allylic alcohols using commercial hydroxylamine-O-sulfonic acid (HOSA)²² and Et₃N to prepare value-added nitrogenous motifs, viz., anilines and/or nitriles in addition to N-heterocycles. Of particular note are applications to cyclic alcohols that result in either symmetrical or unsymmetrical bis-functionalization with their attendant increases in architectural complexity and step-economy.

Results and discussion

Prompted by the above C–C cleavage reports and our prior aryl and alkene amination studies,^17a,18,23 we foresaw (i) the untapped potential to develop novel bis-functionalization applications with attendant improvements in architectural complexity and step-economy, (ii) extension to an additional substrate class, i.e., allylic alcohols, in addition to alkylarenes/styrenes, and (iii) utilization of a more acceptable aminating reagent. To these ends, a mixture of model substrate 1-tetrahydronaphthol (1a, α-tetralol) and aminating reagent hydroxylamine-O-sulfonic acid (HOSA) was screened with a variety of organic/inorganic bases in several common solvents (see ESI†) and discovered to give anilino-nitrile 2a, whose differentiated nitrogen functionality was deemed to hold considerable synthetic potential. Following optimization of reagent ratios (see ESI†), the isolated yield of 2a was raised to 92% using equimolar HOSA and Et₃N in 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) at rt (Table 1); while CsOH as base was comparable to Et₃N, its deliquescence precluded routine use. These studies also revealed that a base for deprotonation of zwitterionic HOSA is crucial for reaction (entry 6). No or little reaction occurred in MeOH, CH₂Cl₂ or THF. For α-tetralol (1a, Table 1), the observed migratory aptitude (aryl ≫ alkyl) correlated with well established migratory aptitudes. Application of these conditions to seven-membered 2-methyl-α-tetralol (1c), and 4-(3,4-dichlorophenyl)-α-tetralol (1d) likewise gave good yields of the corresponding anilino-nitriles 2b–d; of interest, 2d's benzhydryl hydrogen proved stable. Substituents on the aromatic ring also were well tolerated ranging from electron donating groups, viz., free phenol (1e), methoxy (1f), silyl ether (1g), allyl ether (1h) and benzyl ether (1i) to halogens (1j,k) and even the more powerful electron withdrawing groups nitro (1l) and methoxycarbonyl (1m), although the latter two alcohols needed gentle warming to achieve acceptable reaction rates. As an indication of the mild reaction conditions, the labile cis-stilbene 2n was obtained from dibenzosuberenol (1n) without isomerization to the thermodynamically more stable trans-isomer. Other sensitive and/or polyfunctional molecules that proved compatible with the bis-functionalization protocol are evident in 9H-fluoren-9-amide 2o, seco-estradiol dibenzoate 2p, Cbz-protected dipeptide 2q, thiazole 2r, and pyrazine 2s, all of which were realized in good yields. The scope of the site-selective C–C cleavage was further explored using readily available acyclic benzyl alcohols leading to the corresponding anilines (Table 2). Access to aniline itself (4a) and N-methylaniline (4a′) from 1-phenylethanol 3a proceeded smoothly (71% and 72% overall yield, respectively) using HOSA and N-methylhydroxylamine-O-sulphonic acid,²⁴ respectively. Additional substitution at the benzylic position capable of supporting a carbocation, e.g., benzhydrol (3a′) and 2-phenylisopropanol (3a′′), accelerated the reaction rate; the non-migrating phenyl of 3a′ was obtained as a 2 : 1 mixture of benzaldehyde and benzonitrile (54%). Also, moderate to strong electron donating aryl substituents were also more reactive as illustrated in 4b–f, 4s while simultaneously offering comparatively better yields vis-à-vis the hydrazoic acid based procedure;^19,20 even the easily oxidized p-phenylenediamines 4g,h were well behaved. Additionally, examples containing 2-naphthyl 4i, biphenyl 4j, and quinoline 4k as well as typical electron withdrawing substituents such as acetamide 4l, bromide 4m, and nitro 4n delivered the corresponding anilines without incident. For validation within the context of polyfunctional bioactive scaffolds, benzyl alcohols derived from acebutolol, iloperidone, and adapalene were converted to anilines 4o–q. To better understand the reaction course, 3r was treated with 1 equivalent each of HOSA and Et₃N in HFIP as solvent resulting in 4r (45%) and 4-phenylcyclohexanone (38%), most likely arising from hydrolysis of the intermediate imine. As might be expected, acid sensitive functionality such as acetonides and epoxides are not stable under the moderately acidic reaction conditions.

Optimization table of cyclic benzyl alcohols via C–C cleavage^a.

Entry	Photocatalyst (mol%) blue LED (470 nm)	Solvent	Base	Temp. (°C)	Time (h)	Yield (%)
1	[Ir{dF(CF3)ppy}2(dtbpy)PF6 (2)	HFIP	Et3N	—	1	72
2	Eosin-Y	HFIP	Et3N	—	1	70
3	—	HFIP	Et3N	60	1	66
4	[Ir{dF(CF3)ppy}2(dtbpy)]PF6 (2)	CH2Cl2	Et3N	—	24	0
5	—	HFIP	Et 3 N	23	14	92
6	—	HFIP	—	23	14	0
7	—	HFIP	Pyridine	23	14	79
8	—	HFIP	DMAP	23	14	85
9	—	TFE	Et3N	60	24	42
10	—	THE	Et3N	60	24	0
11	—	MeOH	Et3N	60	24	<5
12	—	CH2Cl2	Et3N	60	24	<5

^aSee ESI for additional details.

Bis-functionalization of cyclic benzyl alcohols via C–C cleavage^a,b.

^aReactions conditions: benzyl alcohol (0.5 mmol), H₂NOSO₃H (2.2 equiv.), Et₃N (2.2 equiv.) at 0.15 M in hexafluoroisopropanol (HFIP) under argon.

^bIsolated yields.

^c5 mmol scale. H₂NOSO₃H: hydroxylamine-O-sulfonic acid; HFIP: 1,1,1,3,3,3-hexafluoroisopropanol.

Extension of the bis-functionalization repertoire to cyclic allylic alcohol 5a gave rise to adiponitrile (6a), an industrially important commodity, whereas acyclic 5b led to 2-phenylacetonitrile (6b) (Table 3). On the other hand, a 1 : 2 mixture of 3-phenylpropnitrile (6c) and 4-phenylbutyronitrile (6c′) was obtained from 5c, although in good combined yield. Similarly, a 1 : 1.3 mixture of undecanenitrile (6d) and dodecanenitrile (6d′) was observed coming from 5d reflecting the competing influences of charge distribution in the allylic carbocation vs. steric approach of HOSA. For trisubstituted allylic alcohol 5e, nitrile 6e was the minor product and Beckmann lactam 6e′, resulting from initial addition of HOSA to the tertiary center, was favored. For some cyclic benzylic alcohols (Table 4), arene migration to the HOSA nitrogen (Fig. 2) directly resulted in a stable aromatic system, e.g., phenanthridene (7a) from 9-hydroxyfluorene and dibenzoxazepine (7b) dibenzoxazepine (7b) from xanthydrol. In other systems, aromatization occurred following in situ oxidation of the intermediate imine, e.g., quinoline (7c) from 1-indanol and substituted quinoline 7d; the former via exposure to air during the course of the reaction and the latter induced by HOSA, itself a mild oxidant. Alternatively, the process can be paused after the first rearrangement step by restricting the amount of HOSA/Et₃N and the newly generated imine reduced in situ. For instance, the one-pot, sequential treatment of 1a with just 1.2 equivalents each of HOSA and Et₃N, followed by sodium cyanoborohydride after 1a was consumed, produced 1H-tetrahydrobenzazepine (7e) in 71% yield accompanied by 4a (4%); 2-methyl-1H-tetrahydrobenzazepine (7f; 91%) was secured analogously from 1-methyl-1-tetrahydronaphthol (Table 5).

Synthesis of anilines via C–C cleavage of acyclic benzyl alcohols^a,b.

^aReactions conditions: benzyl alcohol (0.5 mmol), H₂NOSO₃H (1.5 equiv.), Et₃N (1.5 equiv.) at 0.15 M in hexafluoroisopropanol (HFIP) under argon.

^bIsolated yields.

^cFor convenience, isolated as the N-acetamide; overall yield for C–C cleavage and N-acylation.

^dMeHNOSO₃H (3 equiv.) and Et₃N (1.5 equiv.).

^e3 equiv. each of H₂NOSO₃H and Et₃N.

^f1.5 equiv. each of H₂NOSO₃H and Et₃N gave 4m (33%) and unreacted starting material (51%).

^g1.5 equiv. each of H₂NOSO₃H and Et₃N gave 4n (21%) and unreacted starting material (68%).

^hUsing 1 equiv. each of H₂NOSO₃H and Et₃N, 4-phenylcyclohexanone was also isolated in 38% yield.

ⁱUsing 1.5 equiv. each of H₂NOSO₃H and Et₃N, 4-phenylcyclohexanone was also isolated in 45% yield.

Mono-/bis-nitriles via C–C cleavage of allylic alcohols^a,b.

^aReactions conditions: allylic alcohol (0.5 mmol), HOSA (4.0 equiv.), Et₃N (4.0 equiv.) at 0.15 M in hexafluoroisopropanol (HFIP) under argon.

^bIsolated yields.

^cRatio determined via¹H NMR.

^dRatio determined via LC/HRMS.

Fig. 2. Plausible bis-functionalization mechanism. Illustrated for (i) α-tetralol (1 → 2a) and 1-cyclohexenol (5a → 6a) (ii) plausible mechanism for acyclic benzyl alcohols and (iii) control experiment consistent with carbocation intermediacy.

N-Heterocycles from cyclic benzyl alcohols via C–C cleavage^a,b.

^aReactions conditions: isolated yields.

^bBenzyl alcohol (0.5 mmol), HOSA (2.2 equiv.), Et₃N (2.2 equiv.) at 0.15 M in HFIP under argon.

^cConducted open to atmosphere.

^dUsed (i) HOSA (1.2 equiv.) and Et₃N (1.2 equiv.), 0 °C; (ii) NaBH₃CN (2 equiv.), rt.

Control experiments (see ESI†) proved instructive in understanding the plausible mechanism. For example, 2f in HFIP (0.15 M) at rt, but in the absence of HOSA and TEA, formed the corresponding HFIP ether 8 overnight, consistent with the formation of a carbocation intermediate. Treatment of 1a with butylated hydroxytoluene (BHT) under our standard reaction condition resulted in no change in the yield of 2a which doesn't support a long lived radical mechanism. On the other hand, the yield of 2a was significantly decreased in the presence of 2 equiv. of TEMPO; however, control experiments suggested that the HOSA is decomposed by TEMPO under our reaction conditions (see ESI†).

Fig. 2 presents a generalized, mechanistic scenario by which benzylic and allylic alcohols undergo bis-functionalization either type of alcohol is readily converted to the corresponding hydroxylamine-O-sulfonate trimethylamine salt Bvia stabilized carbocation A. Subsequent rearrangement of B forms iminium C that in turn forms D upon addition of a second equivalent of triethylammonium HOSA. For benzyl alcohols, a quick succession of eliminations, firstly to aldoxime E by collapse of the aminal in D, and finally yields anilino-nitrile (illustrated by 2a) via loss of sulfate and a proton. If an allylic alcohol is the substrate, E leads to imine-enamine F that eventually terminates at bis-nitrile (illustrated by 6a) following an addition/elimination sequence similar to the one that led to 2a.

For acyclic benzyl alcohols, iminium intermediate H provided the corresponding anilines and aldehydes/ketones upon aqueous isolation.

Conclusions

The foregoing one-pot methodology exploits the site-selectivity of C(sp²)–C(sp³) cleavage of benzylic and allylic alcohols for non-hazardous, metal-free access to anilines and/or nitriles or, most notably for cyclic systems, to anilino-nitriles and bis-nitriles, respectively, with highly advantageous step and atom efficacy. In preliminary studies, we also sought to extend our methodology to substrates that are otherwise refractory and for this the reaction conditions were conflated with prior methodology.^19,25 Proof of principle was gained using the otherwise unreactive benzyl alcohol (3t) that was converted with commercial N-^tBoc-O-tosylhydroxylamine under Mitsunobu conditions to O-tosyloxime 9 that subsequently underwent rearrangement to aniline (4a) under the influence of trifluoroacetic acid in methanol (eqn (1a), isolated as the N-acetamide) (Table 6).

Synthesis of anilines via C–C cleavage of alkylarenes and primary benzyl alcohols.

Unexpectedly, N-heterocycle (10) was observed (see ESI†) when 9 was stirred with excess TFA in HFIP as solvent (eqn (1b)), presumably involving three successive transformations (C–C cleavage, decarboxylation and rearrangement). α-Unfunctionalized alkylarenes, e.g., 11, are also inert to the standard reaction conditions, but could be coaxed to rearrange using a mixture of DDQ and HOSA/Et₃N (eqn (2)). Detailed studies will appear elsewhere.

Data availability

Data for this work, including optimization tables, general experimental procedures and characterization data for all new compounds are provided in the ESI.†

Author contributions

R. R. A. conceptualized the project, conducted the experiments, analyzed the data and wrote the original draft. J. R. F. provide project supervision and manuscript review.

Conflicts of interest

The authors declare no competing financial interests.