2,4-Dichlorobenzaldehyde → HCID 10188983, compound

HRID 1794199Notes

Reaction equation

HRID 1794199 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][CH:13]=[CH:12]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:18][C:19]1[CH:26]=[C:25]([Cl:27])[CH:24]=[CH:23][C:20]=1[CH:21]=O>>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][CH:13]=[C:12]2[CH:21]([C:12]1[C:11]2[C:15](=[CH:16][CH:17]=[C:9]([O:8][CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[CH:10]=2)[NH:14][CH:13]=1)[C:20]1[CH:23]=[CH:24][C:25]([Cl:27])=[CH:26][C:19]=1[Cl:18])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 134042,4-DichlorobenzaldehydeHCID 146245-Benzyloxyindole

Product 1

HCID 10188983HCID 10188983, compound

Procedure

The compound Bis(5-benzyloxyindol-3-yl)-(2,4-dichlorophenyl)methane was prepared following procedure A, starting from 5-benzyloxy indole and 2,4 dichloro benzaldehyde. LC: Tr 2.89 min, MS: 603 (M+H)+

Workup

  1. customTr 2.89 min, MS

Sources & evidence

ORD record
ord-d9da5db6e29644419f37410debfa0467
Source dataset
uspto-grants-2006_04
Patent number
US07022730B2

Reaction notes

Loading…