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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497141Generated: October 25, 2026

1,2-Dichloroethane → 4-Chlorobenzhydrol

https://huagongshe.com/reaction/497141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantNorchlorcyclizineHCID 9340—
ReactantDiphenylpropionic acidHCID 64798—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-ChlorobenzhydrolHCID 840178%

Reaction Steps

To a solution of 1-[(4-chloro-phenyl)-phenyl-methyl]-piperazine (0.59 g, 2.08 mmol) in dry CH2Cl2 (40 ml) was added 3,3-diphenylpropanoic acid (0.472 g, 2.08 mmol) under nitrogen. To the reaction was added EDC (0.797 g, 4.16 mmol) and DMAP (cat) and the reaction mixture stirred under nitrogen at room temp. over night. The reaction was then concentrated under reduced pressure. The residue dissolved in ethyl acetate: water (10:1) (150 ml). The organic was washed with water (30 ml, 2×) and 10% NaOH (30 ml) and dried over MgSO4 and evaporated to dryness. The resulting residue was purified by column chromatography using hexane: ethyl acetate (3:1) to give desired product in 78% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949554B2
Source datasetuspto-grants-2005_09
ORD IDord-8880e1cd7dbf471a8968b80625732fc8
Source noteuspto-grants-2005_09