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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407960Generated: October 30, 2026

Oxalyl chloride → Tert-butyl 3-(3-(chlorocarbonyl)benzylthio)propanoate

https://huagongshe.com/reaction/1407960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-((3-Tert-butoxy-3-oxopropylthio)methyl)benzoic acidHCID 66586713—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 3-(3-(chlorocarbonyl)benzylthio)propanoateHCID 86705208—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 100-mL round-bottom flask, was placed a solution of 3-((3-tert-butoxy-3-oxopropylthio)methyl)benzoic acid 1.1c (3.00 g, 10.14 mmol, 1.00 equiv) in dichloromethane (50 mL). This was followed by the addition of oxalyl dichloride (4.50 g, 35.43 mmol, 3.00 equiv) dropwise with stirring at 0° C. To this was added N,N-dimethylformamide (one drop). The resulting solution was stirred for 1.5 h at room temperature. The resulting mixture was concentrated under vacuum. This resulted in 3.18 g (99%) of tert-butyl 3-(3-(chlorocarbonyl)benzylthio)propanoate as red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916569B2
Source datasetuspto-grants-2014_12
ORD IDord-61b9d039c855453ebe078f51c0169654
Source noteuspto-grants-2014_12