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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591617Generated: November 2, 2026

Methanol → Methyl 5-bromo-2-chlorobenzoate

https://huagongshe.com/reaction/1591617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant5-Bromo-2-chlorobenzoic acidHCID 33127—
ReactantOxalyl chlorideHCID 65578—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-bromo-2-chlorobenzoateHCID 84209891%

Reaction Steps

To a suspension of 5-bromo-2-chloro-benzoic acid (2.5 g, 10.6 mmol) in dichloromethane (50 ml) was added a solution of oxalyl chloride in dichloromethane (2 M, 6 ml, 12 mmol) followed by N,N-dimethylformamide (5 drops). After stirring for 30 minutes, methanol (10 ml) was added and the mixture was stirred for 20 hours. The mixture was concentrated under reduced pressure and partitioned between ethyl acetate (150 ml) and saturated aqueous potassium carbonate solution (100 ml). The organic layer was concentrated under reduced pressure to provide methyl 5-bromo-2-chloro-benzoate (2.4 g, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291616B2
Source datasetuspto-grants-2007_11
ORD IDord-37cbd43736b94d348c09fd19a11e55af
Source noteuspto-grants-2007_11