p-Bromobenzyl chloride → HCID 23350213, compound
Reaction equation
[Cl:1][C:2]1[CH:17]=[C:16]([Cl:18])[C:15]([Cl:19])=[CH:14][C:3]=1[NH:4][CH2:5][CH:6]([OH:13])[CH2:7][N:8]1[CH:12]=[CH:11][N:10]=[CH:9]1.[Br:20][C:21]1[CH:28]=[CH:27][C:24]([CH2:25]Cl)=[CH:23][CH:22]=1>>[Br:20][C:21]1[CH:28]=[CH:27][C:24]([CH2:25][O:13][CH:6]([CH2:5][NH:4][C:3]2[CH:14]=[C:15]([Cl:19])[C:16]([Cl:18])=[CH:17][C:2]=2[Cl:1])[CH2:7][N:8]2[CH:12]=[CH:11][N:10]=[CH:9]2)=[CH:23][CH:22]=1Participants
3
Procedure
Reaction of 1-[3-(2,4,5-trichloroanilino)-2-hydroxypropyl]-imidazole with p-bromobenzyl chloride yields 1-[2-(4-bromobenzyloxy)-3-(2,4,5-trichloroanilino)-propyl]-imidazole.
Sources & evidence
- ORD record
- ord-7083a5f684bd4e59a77489ea962bbb3e
- Source dataset
- uspto-grants-1980_07
- Patent number
- US04215220
Reaction notes
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