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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280852Generated: October 29, 2026

Benzoyl chloride → HCID 23320196, compound

https://huagongshe.com/reaction/280852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantFumaric AcidHCID 444972—
ReactantHCID 19370338HCID 19370338—
SolventChloroformHCID 6212—
ProductHCID 23320196HCID 23320196—

Reaction Steps

To a solution of 1-(3-aminopropyl)-4-(4-chlorobenzhydryl)piperazine (1.7 g) and triethylamine (0.7 g) in chloroform (20 ml) was dropwise added benzoyl chloride (0.7 ml) at ambient temperature and the mixture was stirred at the same temperature for 1.5 hours. The reaction mixture was washed successively with aqueous sodium bicarbonate and water, and then extracted with 10% hydrochloric acid. After neutralizing the aqueous extract with aqueous sodium carbonate, the desired product was extracted with ethyl acetate. The organic extract was washed with water, dried and evaporated in vacuo to give an oil. According to a conventional manner, the oily product was converted to fumaric acid salt, which was recrystallized from a mixture of ethanol and diethyl ether to afford 1-(3-benzoylaminopropyl)-4-(4-chlorobenzhydryl)piperazine fumarate (0.82 g) as white crystals. mp: 173°-175° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04591590
Source datasetuspto-grants-1986_05
ORD IDord-5268feb9bfec4d1d9eb5919a79aa3ba7
Source noteuspto-grants-1986_05