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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406069Generated: October 31, 2026

Oxalyl chloride → Methyl 3-(3-(chlorocarbonyl)benzylthio)propanoate

https://huagongshe.com/reaction/2406069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-((3-Methoxy-3-oxopropylthio)methyl)benzoic acidHCID 43408254—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-(3-(chlorocarbonyl)benzylthio)propanoateHCID 8670520291.7%

Reaction Steps

Into a 50-mL round bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 3-((3-methoxy-3-oxopropylthio)methyl)benzoic acid (61.6 mg, 0.24 mmol, 1.00 equiv) in dichloromethane (5 mL). This was followed by dropwise addition of oxalyl dichloride (121.76 mg, 0.96 mmol, 4.00 equiv) with stirring at room temperature. Then a few drops of N,N-dimethylformamide were added as catalyst. The resulting solution was heated to reflux for 30 min. The resulting mixture was concentrated under vacuum to yield 60 mg (crude) of methyl 3-(3-(chlorocarbonyl)benzylthio)propanoate as yellow oil. The crude was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809339B2
Source datasetuspto-grants-2014_08
ORD IDord-ec000f5f55d64c1ba9a5ae3e713ab2b6
Source noteuspto-grants-2014_08