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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888565Generated: October 25, 2026

Hydrochloric Acid → 4-Bromo-phenyl-3-(4-chloro-phenyl)-2-cyano-propionic acid ethyl ester

https://huagongshe.com/reaction/888565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantEthyl 3-(4-bromophenyl)-2-cyanoprop-2-enoateHCID 367501—
ReactantHCID 178478191HCID 178478191—
Product4-Bromo-phenyl-3-(4-chloro-phenyl)-2-cyano-propionic acid ethyl esterHCID 8665432391%

Reaction Conditions

Temperature85 °C

Reaction Steps

A solution of 3-(4-bromo-phenyl)-2-cyano-acrylic acid ethyl ester (1.5 g, 5.36 mmol) in dry toluene (12 ml) was added dropwise to 4-chlorophenylmagnesium bromide (0.5 M solution in tetrahydrofuran, 6.96 ml, 6.96 mmol) at 0° C. The reaction mixture was heated to 85° C. for 3 hours, poured onto ice, acidified with 1N HCl and extracted with ethyl acetate. The organic layer was separated, dried (MgSO4), filtered and concentrated, the crude product was purified over flash silica chromatography eluting with petroleum ether to ethyl acetate/petroleum ether (5:95) to afford the desired product (1.91 g, 91% yield). LC/MS: (PS-A2) Rt 3.78 [M+H]− 391.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247576B2
Source datasetuspto-grants-2012_08
ORD IDord-3e3e21ab170d41c7a5c51f7e0b7c237d
Source noteuspto-grants-2012_08