Aluminum;lithium → {1-benzyl-5-[4-(trifluoromethoxy)phenyl]-1H-indol-2-yl)methanol

HRID 2212149Notes

Reaction equation

HRID 2212149 reaction equation
[CH2:1]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([C:17]3[CH:22]=[CH:21][C:20]([O:23][C:24]([F:27])([F:26])[F:25])=[CH:19][CH:18]=3)=[CH:14][CH:15]=2)[CH:10]=[C:9]1[C:28](OCC)=[O:29])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Al].[Li]>>[CH2:1]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([C:17]3[CH:22]=[CH:21][C:20]([O:23][C:24]([F:27])([F:25])[F:26])=[CH:19][CH:18]=3)=[CH:14][CH:15]=2)[CH:10]=[C:9]1[CH2:28][OH:29])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 16211445Aluminum;lithiumHCID 21964294Ethyl 1-benzyl-5-[4-(trifluoromethoxy)phenyl]-1H-indole-2-carboxylate

Product 1

HCID 21964310{1-benzyl-5-[4-(trifluoromethoxy)phenyl]-1H-indol-2-yl)methanol

Procedure

The title compound was prepared from ethyl 1-benzyl-5-[4-(trifluoromethoxy)phenyl]-1H-indole-2-Carboxylate (step 3 of Example 1) and lithium aluminum in substantially the same manner, as described in step 1 of Example 21. The product was obtained as a white solid, mp: 108–109° C. Mass spectrum (ESI, [M+H]+) m/z 398. 1H NMR (400 MHz, DMSO-d6) δ 7.82 (s, 1H), 7.76 (d, 2H, J=8.86 Hz), 7.42–7.36 (m, 4H) 7.29 (d, 1H, J=7.03 Hz), 7.27 (d, 1H, J=7.63 Hz), 7.23–7.20 (m, 1H), 7.06 (d, 2H, J=7.03 Hz), 6.52 (s, 1H), 5.50 (s, 2H), 5.36 (t, 1H), and 4.60 ppm (d, 2H).

Workup

  1. customThe product was obtained as a white solid, mp: 108–109° C

Sources & evidence

ORD record
ord-eab901a3f0014a7cb19538b0acdb2c9e
Source dataset
uspto-grants-2006_09
Patent number
US07101903B2

Reaction notes

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