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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1816794Erstellt: 27. Oktober 2026

Thionyl Chloride → 4-Chlorocinnamoyl chloride

https://huagongshe.com/reaction/1816794

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
Edukt4-Chlorocinnamic acidHCID 637797—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelBenzeneHCID 241—
Produkt4-Chlorocinnamoyl chlorideHCID 53411294100,4%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06884890B2
Quelldatensatzuspto-grants-2005_04
ORD IDord-bcb4e4038c8d4deb85065412d76a4aed
Quellennotizuspto-grants-2005_04