Bromine → HCID 13064247, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:28])=[C:6]([CH:27]=1)[CH2:7][C:8]1[CH:13]=[C:12]([F:14])[CH:11]=[C:10]([CH:15]([C:17]2[CH:22]=[C:21]([Cl:23])[CH:20]=[C:19]([Cl:24])[C:18]=2[OH:25])[CH3:16])[C:9]=1[OH:26].[Br:29]Br>C(O)(=O)C>[Br:29][C:4]1[C:5]([OH:28])=[C:6]([CH:27]=[C:2]([Cl:1])[CH:3]=1)[CH2:7][C:8]1[CH:13]=[C:12]([F:14])[CH:11]=[C:10]([CH:15]([C:17]2[CH:22]=[C:21]([Cl:23])[CH:20]=[C:19]([Cl:24])[C:18]=2[OH:25])[CH3:16])[C:9]=1[OH:26]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-(5-Chloro-2-hydroxybenzyl)-6-[1-(3,5-dichloro-2-hydroxyphenyl) ethyl]-4-fluorophenol was brominated using bromine in acetic acid at room temperature to give the title compound; m.p. 171°.
Workup
- customat room temperature
Sources & evidence
- ORD record
- ord-a0eea2d9b9434e33a0f61aaf592e1c24
- Source dataset
- uspto-grants-1979_08
- Patent number
- US04163801
Reaction notes
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