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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230215Generated: October 26, 2026

Methanol → Methyl 5-chloro-2-methylbenzoate

https://huagongshe.com/reaction/230215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Chloro-2-methylbenzoic acidHCID 82009—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-chloro-2-methylbenzoateHCID 2045960096%

Reaction Steps

5-Chloro-2-methylbenzoic acid (46, 5.0 g, 29.3 mmol) was suspended in dichloromethane (30 mL) and thionyl chloride (3.2 mL, 5.2 g, 44 mmol) was added. The solution was stirred at room temperature for 1 hour. Methanol was added and the reaction was allowed to proceed for a further 16 hours. The volatile components were evaporated under reduced pressure. The resulting residue was taken up again in methanol (30 mL) and pyridine (5 mL) was added. The solution was stirred at room temperature for 2 days. The solvent was evaporated under reduced pressure. The residue was dissolved in dichloromethane and washed with water. The organic phase was dried over anhydrous magnesium sulfate, filtered, and concentrated to afford methyl 5-chloro-2-methylbenzoate (5.3 g, 96% yield) that was used in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566718B2
Source datasetuspto-grants-2009_07
ORD IDord-538cf47b08b349e39490757c6154a296
Source noteuspto-grants-2009_07