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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816794Generated: October 26, 2026

Thionyl Chloride → 4-Chlorocinnamoyl chloride

https://huagongshe.com/reaction/1816794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-Chlorocinnamic acidHCID 637797—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventBenzeneHCID 241—
Product4-Chlorocinnamoyl chlorideHCID 53411294100.4%

Reaction Steps

3-(4-chloro-phenyl)-acryloyl chloride was prepared as follows: To a stirred suspension of 4-chloro-trans-cinnamic acid (251 g, 13.77 mmol) in benzene was added thionyl chloride (1.1 mL, 15.14 mmol) and a catalytic amount of DMAP. The reaction mixture was heated at reflux for 1.5 h. The volatile materials were removed under reduced pressure. The white residue was dissolved in Et2O and concentrated again under reduced pressure, to give 3-(4-chloro-phenyl)-acryloyl chloride (2.78 g, quantitative) as a white solid: 1H NMR (CDCl3) δ 7.81 (d, 1H, 1=15.6 Hz), 7.54 (d, 2H, J=8.6 Hz), 7.44 (d, 2H, J=8.6 Hz), 6.65 (d, 1H, J=15.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884890B2
Source datasetuspto-grants-2005_04
ORD IDord-bcb4e4038c8d4deb85065412d76a4aed
Source noteuspto-grants-2005_04