HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113871Generated: October 31, 2026
Ammonia → 3-(4-Trifluoromethylsulfanyl-phenyl)-acrylamide
https://huagongshe.com/reaction/2113871
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-{4-[(Trifluoromethyl)sulfanyl]phenyl}prop-2-enoic acid | HCID 53395635 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Trifluoromethylsulfanyl-phenyl)-acrylamide | HCID 69112057 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432291B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-285b7ee0832c44fabc0d755dc07bcecb |
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| Source note | uspto-grants-2008_10 |
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