HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184528Generated: November 1, 2026
3-Chloroaniline → (E)-N-(3-Chloro-phenyl)-3-(3-hydroxy-phenyl)-acrylamide
https://huagongshe.com/reaction/1184528
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloroaniline | HCID 7932 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-coumaric acid, (E)- | HCID 637541 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (E)-N-(3-Chloro-phenyl)-3-(3-hydroxy-phenyl)-acrylamide | HCID 45376336 | 8.4% |
Reaction Steps
A solution of (E)-3-(3-hydroxy-phenyl)-acrylic acid (1.0 g, 6.1 mmol) and thionyl chloride (0.53 mL, 7.32 mmol) in dry THF (15 mL) was stirred at 55° C. for 3 hrs. Then a further aliquot of thionyl chloride (0.1 mL, 1.38 mmol) is added and the mixture is stirred at reflux temperature for additional 1.5 hrs. After cooling to about 5° C., a solution of 3-chloro-aniline (0.65 mL, 6.1 mmol) and triethylamine (3.4 mL, 24.4 mmol) in dry THF (5 mL) was added dropwise. After stirring at RT for 16 hrs the reaction mixture was diluted with DCM and washed with water, aqueous hydrochloric acid, and brine. The organic layer was dried over sodium sulphate and evapored. The resulting raw material was purified first by column chromatography (eluant petroleum ether/AcOEt 45/55) and then by trituration in DCM, yielding 140 mg of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08669261B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-a50b22a682a34ae3afc2b9031bf05ee0 |
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| Source note | uspto-grants-2014_03 |
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