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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260374Generated: November 1, 2026

3-Chloroaniline → (E)-N-(3-Chloro-phenyl)-3-(3-hydroxy-phenyl)-acrylamide

https://huagongshe.com/reaction/1260374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloroanilineHCID 7932—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant3-coumaric acid, (E)-HCID 637541—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(E)-N-(3-Chloro-phenyl)-3-(3-hydroxy-phenyl)-acrylamideHCID 453763368.4%

Reaction Conditions

Temperature5 °C

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 evaporated. 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470831B2
Source datasetuspto-grants-2013_06
ORD IDord-0c949cdbc3e14b8a9a402266e438d3ca
Source noteuspto-grants-2013_06