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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916677Generated: October 26, 2026

Isopropanol → Methyl 4-[(2-chloroethyl)thio]butanoate

https://huagongshe.com/reaction/916677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium hydrideHCID 24758—
Reactant4-Mercaptobutanoic acidHCID 25700—
ProductMethyl 4-[(2-chloroethyl)thio]butanoateHCID 22592554—

Reaction Steps

A 0° C. isopropanol (70 mL) solution of 4-mercaptobutyric acid (3.85 g, 20 mmol) was treated with sodium hydride in four portions (95%, 1.56 g total, 65 mmol) over 20 minutes and allowed to warm to room temperature. 1-Bromo-2-chloroethane (11 mL, 128 mmol) was added rapidly with the resulting suspension stirred vigorously for 2 days, then the volatiles were removed, and the residue was partitioned between 5% aqueous acetic acid and ethyl acetate. The combined organic extracts were washed with brine and stored over sodium sulfate. The extract was filtered and the volatiles were removed under vacuum. The residue was dissolved in methanol (60 mL) and cooled to 0° C. under argon atmosphere. Thionyl chloride (5 mL, 69 mmol) was added dropwise and the solution was stirred at room temperature. After 2-3 hours, the volatiles were removed, toluene was added, and the volatiles were removed again. Chromatography yielded (2.93 g, 14 mmol) of methyl 4-[(2-chloroethyl)thio]butanoate as a colorless oil: MS (NH3) m/z 199 (M+1+ with 37Cl), 197 (M+1+ with 35Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271183B2
Source datasetuspto-grants-2007_09
ORD IDord-d7ba431fa6c54ed3afad2238ea074794
Source noteuspto-grants-2007_09