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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861062Generated: November 3, 2026

Thionyl Chloride → 4-Chlorocinnamoyl chloride

https://huagongshe.com/reaction/1861062

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 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, 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 numberUS06531491B1
Source datasetuspto-grants-2003_03
ORD IDord-3a8a1add4bea42bfb6987c4c50e454d4
Source noteuspto-grants-2003_03