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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591632Generated: November 1, 2026

Methanol → Methyl 2-chloro-5-methylbenzoate

https://huagongshe.com/reaction/1591632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Chloro-5-methylbenzoic AcidHCID 240430—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-chloro-5-methylbenzoateHCID 57362636100%

Reaction Steps

To a suspension of 2-chloro-5-methyl-benzoic acid (3.0 g, 17.6 mmol) in dichloromethane (50 ml) was added a solution of oxalyl chloride in dichloromethane (2 M, 10 ml, 20 mmol) followed by N,N-dimethylformamide (5 drops). After stirring for 1 hour, methanol (20 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-chloro-5-methyl-benzoate (3.2 g, 100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291616B2
Source datasetuspto-grants-2007_11
ORD IDord-601f927643b847fbbaf4ec9263c6eee0
Source noteuspto-grants-2007_11