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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361760Generated: November 1, 2026

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

https://huagongshe.com/reaction/2361760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 3-(4-bromophenyl)-2-cyanoprop-2-enoateHCID 367501—
ReactantHCID 178478191HCID 178478191—
SolventTolueneHCID 1140—
Product3-(4-Bromo-phenyl)-3-(4-chloro-phenyl)-2-cyano-propionic acid ethyl esterHCID 5769139791%

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 numberUS08691806B2
Source datasetuspto-grants-2014_04
ORD IDord-b71ddd32a0c245059ce56c0fb61a639d
Source noteuspto-grants-2014_04