4-Bromophenol → HCID 68711019, compound

HRID 1787088Notes

Reaction equation

HRID 1787088 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]=1

Participants

4

Reactant 2

HCID 78084-BromophenolHCID 23423233Hydroxy(4-isopropylphenyl)acetic acid

Product 1

HCID 68711019HCID 68711019, compoundYield 30%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

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-c742566f1151421f8fc9dceb5b8cab0d
Source dataset
uspto-grants-2009_03
Patent number
US07507841B2

Reaction notes

Loading…