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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1813946Generated: October 26, 2026

4-Aminobenzophenone → 4-(4-Chloro-1,2-diphenyl-but-1-enyl)phenylamine

https://huagongshe.com/reaction/1813946

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzophenoneHCID 14346—
Reactant3-ChloropropiophenoneHCID 70295—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
SolventPotassium CarbonateHCID 11430—
Product4-(4-Chloro-1,2-diphenyl-but-1-enyl)phenylamineHCID 69544499—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Zinc (10.0 g, 0.154 mol) and tetrahydrofuran (THF) (120 ml) is added to the reaction vessel and cooled to −10° C. To the mixture is added dropwise titan tetrachloride (1 4.4 g, 0.076 mol) at about −10° C. After the addition is completed the mixture is refluxed for two hours. Then it is cooled to 40° C. and (4-Amino-phenyl)phenyl-methanone (5.1 g, 0.0258 mol) and 3-chloropropiophenone (4.36 g, 0.0258 mol) are dissolved in THF (50 ml) and added to the mixture. Refluxingis continued for additional 3.5 hours. The cooled reaction mixture is poured in aqueous potassium carbonate solution (14 g K2CO3+140 ml water) and allowed to stand over night. The mixture is filtered and the precipitate is washed three times with THF. The filtrate is evaporated to dryness. The residue is dissolved in ethyl acetate and washed with water. Yield 9.6 g Z-isomer being the only isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875775B2
Source datasetuspto-grants-2005_04
ORD IDord-08d59043c5aa49b89af19887374c2c82
Source noteuspto-grants-2005_04