p-Anisoyl chloride → 2-(4-Methoxybenzoyl)-5-methylbenzoic acid

Reaction equation

[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7](Cl)=[O:8])=[CH:5][CH:4]=1.Br[C:13]1[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][C:14]=1[C:15]([OH:17])=[O:16]>>[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([C:13]2[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][C:14]=2[C:15]([OH:17])=[O:16])=[O:8])=[CH:5][CH:4]=1

Participants

Reactant 2

HCID 7477p-Anisoyl chloride

HCID 2280802-Bromo-5-methylbenzoic acid

Product 1

HCID 692118002-(4-Methoxybenzoyl)-5-methylbenzoic acid

Procedure

This compound is obtained according to the procedure described in 1.1. by reacting 4-methoxybenzoyl chloride and 2-bromo-5-methylbenzoic acid after halogen-lithium exchange. It is used in crude form in the following reaction.

Workup

customThis compound is obtained
customin the following reaction

Sources & evidence

ORD record: ord-42bdeafb19fa4f718e1042462480da8c
Source dataset: uspto-grants-2008_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07423030B2

Reaction notes

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