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. Author manuscript; available in PMC: 2015 Jun 1.
Published in final edited form as: Chem Sci. 2014 Mar 28;5(6):2422–2427. doi: 10.1039/C4SC00697F

Table 1.

Amination of Benzaldehyde (1a) with Pentafluorophenyl Azide (2a) Catalyzed by [Co(Por)]a

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entry catalyst temp (°C) solvent yield (%)b
1 [Co(P1)] 80 PhH 56
2 [Co(P1)] 80 PhCl 77
3 [Co(P1)] 80 4-CF3C6H4Cl 71
4 [Co(P1)] 80 PhF 56
5 [Co(P1)] 80 hexane 69
6 [Co(P1)] 80 ClCH2CH2Cl 65
7 [Co(P1)] 40 PhCl trace
8 [Co(TPP)] 80 PhCl trace
9 - 80 PhCl NRc
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a

All reactions were carried out with 1.0 equiv. of aldehyde (0.2 M) and 1.2 equiv. of azide using 3 mol % [Co(Por)] as catalyst.

b

19F-NMR yields.

c

NR = no reaction.