Methyl 4-(bromomethyl)benzoate → HCID 86624410, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([O:11][CH2:12][CH3:13])[C:9]=1[OH:10])[CH:5]=[O:6].[CH3:14][O:15][C:16](=[O:25])[C:17]1[CH:22]=[CH:21][C:20]([CH2:23]Br)=[CH:19][CH:18]=1>>[CH3:14][O:15][C:16](=[O:25])[C:17]1[CH:22]=[CH:21][C:20]([CH2:23][O:10][C:9]2[C:8]([O:11][CH2:12][CH3:13])=[CH:7][C:4]([CH:5]=[O:6])=[CH:3][C:2]=2[Br:1])=[CH:19][CH:18]=1Participants
3
Procedure
Alkylation of 3-bromo-5-ethoxy-4-hydroxy benzaldehyde (4 g) with 4-bromomethylbenzoic acid methyl ester (3.73 g) was performed according to the method described in example 1a. Yield: 6.4 g. MS-ESI: [M+H]+=393/395
Sources & evidence
- ORD record
- ord-dbd482c8f9054fa3acc7f2edb494b19a
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08022218B2
Reaction notes
Loading…