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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265444Generated: November 2, 2026

Methanol → HCID 12067651, compound

https://huagongshe.com/reaction/1265444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant3-Chloro-4-(methylthio)phenylacetic acidHCID 12067650—
ProductHCID 12067651HCID 1206765185.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of (3-chloro-4-methylsulfanyl-phenyl)-acetic acid (8.00 g, 36.92 mmol) in methanol (200 mL) was treated slowly with concentrated sulfuric acid (1 mL). The resulting reaction mixture was heated under reflux overnight. The reaction mixture was allowed to cool to 25° C. and then concentrated in vacuo to remove methanol. The resulting residue was dissolved with ethyl acetate (50 mL). The organic layer was washed with water (1×50 mL). The water layer was further extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with a saturated aqueous sodium bicarbonate solution (1×25 mL). The organic layer was then dried over sodium sulfate, filtered, and concentrated in vacuo to afford (3-chloro-4-methylsulfanyl-phenyl)-acetic acid methyl ester (7.28 g, 85.5%) as a yellow oil which was used without further purification: EI-HRMS m/e calcd for C10H11ClO2S (M+) 230.0168, found 230.0166.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545155B2
Source datasetuspto-grants-2003_04
ORD IDord-184f13ca676542a2b4bc21a8fc5ed096
Source noteuspto-grants-2003_04