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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113871Generated: October 31, 2026

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

https://huagongshe.com/reaction/2113871

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-dimethylformamide a solution of 2.70 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 dried at 40° C. in vacuo. Yield 4.62 g (89%) 3-(4-Trifluoromethylsulfanyl-phenyl)-acrylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432291B2
Source datasetuspto-grants-2008_10
ORD IDord-285b7ee0832c44fabc0d755dc07bcecb
Source noteuspto-grants-2008_10