Table 3.
Substrate scope of the reaction with indoles.a
![]() | ||||
Indoles | Trifluoromethly substituted hydroxylakylated indoles | Mp (°C) | Purity (%)b | Yield (%)c |
![]() 1b |
![]() 3p |
122–124 (75)d [25] |
98 | 96 (95)e [25] |
![]() 1c |
![]() 3q |
160–161 | 99 | 79 |
![]() 1d |
![]() 3r |
192–193 | 97 | 90 |
![]() 1e |
![]() 3s |
112–113 | 99 | 94 (98)e [24] |
![]() 1f |
![]() 3t |
90–91 (90)d [24] |
99 | 96 (98)e [24] |
![]() 1g |
![]() 3u |
165–166 | 98 | 91 |
![]() 1h |
![]() 3v |
227–228 | 97 | 92 |
![]() 1i |
![]() 3w |
239–240 | 99 | 97 |
![]() 1j |
![]() 3x |
185–186 185d [24] |
97 | 90 86e [24] |
aReaction conditions: 1 (3.4 mmol) and 2 (3.75 mmol) in water (5 mL). bPurity was determined by HPLC coupled to a UV diode array detector (DAD) at 220−400 nm. cIsolated yields. dReported melting points. eReported yields.