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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435766Generated: November 3, 2026

Methanol → Methyl 2-bromo-5-methylbenzoate

https://huagongshe.com/reaction/1435766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Bromo-5-methylbenzoic acidHCID 228080—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-bromo-5-methylbenzoateHCID 1511099699%

Reaction Steps

To a suspension of 2-bromo-5-methyl-benzoic acid (3.0 g, 14 mmol) in dichloromethane (100 ml) was added a solution of oxalyl chloride in dichloromethane (2 M, 8 ml, 16 mmol) followed by N,N-dimethylformamide (5 drops). After stirring for 30 minutes, methanol (15 ml) was added. After stirring for 3 hours, the mixture was concentrated under reduced pressure. The residue was partitioned between ethyl acetate (200 ml) and saturated aqueous potassium carbonate solution (100 ml). The organic layer was concentrated under reduced pressure to provide methyl 2-bromo-5-methyl-benzoate (3.2 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618968B2
Source datasetuspto-grants-2009_11
ORD IDord-3e73fdbc3709482490aef7a11a7eeae0
Source noteuspto-grants-2009_11