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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750940Generated: November 1, 2026

Ammonia → 3-(4-Trifluoromethylsulfanyl-phenyl)-acrylamide

https://huagongshe.com/reaction/750940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantOxalyl chlorideHCID 65578—
Reactant3-{4-[(Trifluoromethyl)sulfanyl]phenyl}prop-2-enoic acidHCID 53395635—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Trifluoromethylsulfanyl-phenyl)-acrylamideHCID 69112057—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a suspension of 5.24 g (21.1 mmol) 3-(4-trifluoromethylsulfanyl-phenyl)-acrylic acid in 30.0 ml tetrahydrofuran and 0.3 ml N,N-dimethyl formamide a solution of 2.75 ml (32.0 mmol) oxalyl chloride in 5.0 ml tetrahydrofuran was added dropwise at 0° C. within 20 min. Stirring was continued at 0-5° C. for 30 min. and 3 h at room temperature thereafter. The resulting solution was cooled to 0-5° C. again and then added within 15 min. to 100 ml of a 25% aqueous ammonia solution. After evaporation of the organic solvent, 200 ml water were added and the solution cooled. The precipitated amide was collected, washed with water and n-heptane and dried at 40° C. in vacuo. Yield 4.62 g (86%) 3-(4-trifluoromethylsulfanyl-phenyl)-acrylamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405231B2
Source datasetuspto-grants-2008_07
ORD IDord-3d84af41fc934b4485f1a8a56fde5960
Source noteuspto-grants-2008_07