4-Bromophenol → HCID 68711019, compound
Reaction equation
O[CH:2]([C:6]1[CH:11]=[CH:10][C:9]([CH:12]([CH3:14])[CH3:13])=[CH:8][CH:7]=1)[C:3]([OH:5])=[O:4].[Br:15][C:16]1[CH:21]=[CH:20][C:19](O)=[CH:18][CH:17]=1>CO>[Br:15][C:16]1[CH:17]=[CH:18][C:19]2[O:5][C:3](=[O:4])[CH:2]([C:6]3[CH:11]=[CH:10][C:9]([CH:12]([CH3:14])[CH3:13])=[CH:8][CH:7]=3)[C:20]=2[CH:21]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Using hydroxy(4-isopropylphenyl)acetic acid synthesized in Reference Example 1 and 4-bromophenol, the title compound was synthesized in the same manner as in Reference Example 2. Yield 30%. Melting point: 157-158° C. (methanol).
Sources & evidence
- ORD record
- ord-87e6e634cb784a259a78d63fd8a33f07
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07465815B2
Reaction notes
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