Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181507Generated: October 30, 2026

Thionyl Chloride → 4-Chlorocinnamoyl chloride

https://huagongshe.com/reaction/2181507

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 (2.51 g, 13.77 mmol) in benzene was added thionyl chloride (1.1 mL, 15.14 mmol) and a catalylic 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, J=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 numberUS06891044B2
Source datasetuspto-grants-2005_05
ORD IDord-12b1e6d5cb0b4f338d2c0553a63f4247
Source noteuspto-grants-2005_05