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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351794Generated: October 30, 2026

Dimethylformamide → 5-Chloro-2-(3,4,4-trifluoro-3-butenylthio)oxazole

https://huagongshe.com/reaction/351794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSulfuryl chlorideHCID 24648—
Reactant2-(3,4,4-Trifluoro-3-butenylthio)oxazoleHCID 12993958—
SolventChloroformHCID 6212—
Product5-Chloro-2-(3,4,4-trifluoro-3-butenylthio)oxazoleHCID 1299396151.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

4.0 g of 2-(3,4,4-trifluoro-3-butenylthio)oxazole was added to 40 ml of DMF (dehydrated) to which a mixture of 10 ml of chloroform and 2.6 g of sulfuryl chloride was added dropwise at 50 in 1 hour. After the reaction mixture was stirred at 50° C. for 3 hours, a mixture of 5 ml of chloroform and 0.8 g of sulfuryl chloride was further added dropwise in 15 minutes. After stirring at 50° C. for 15 hours, the reaction mixture was cooled to room temperature, poured into 200 ml of ice water and extracted with 100 ml of hexane. The aqueous layer was neutralized with 1N aqueous solution of sodium hydroxide and further extracted with 100 ml of hexane. The extracted hexane layers were put together, washed with 200 ml of saturated common salt water and dried with magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was purified by column chromatography (eluent: hexane:dichloromethane=1:1) to obtain 2.4 g of 5-chloro-2-(3,4,4-trifluoro-3-butenylthio)oxazole as colorless oil (yield 51.5%, n20D=1.4830).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743814B2
Source datasetuspto-grants-2004_06
ORD IDord-61eb23639a4f4fb7b77448f5f7478633
Source noteuspto-grants-2004_06