Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389050Generated: November 1, 2026

Benzoyl chloride → {4-[2-(6-Methoxynaphthalen-2-yl)propyl]piperazin-1-yl}(phenyl)methanone

https://huagongshe.com/reaction/1389050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantEthylmorpholineHCID 7525—
ReactantHCID 3055305HCID 3055305—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product{4-[2-(6-Methoxynaphthalen-2-yl)propyl]piperazin-1-yl}(phenyl)methanoneHCID 3055311—

Reaction Steps

Benzoyl chloride (0.58 ml, 5 mmols) is added, at 0° C., to a solution of 2-(2-piperazino-1-methylethyl)-6-methoxynaphthalene (1.42 g, 5 mmols) and N-ethylmorpholine (0.65 ml, 5 mmols) in 15 ml of methylene chloride. The mixture is allowed to return to ambient temperature and stirred for 3 hours. The reaction medium is washed with water and dried over sodium sulphate. Concentration of the mixture yields an oily residue which dissolves in ether and crystallises. The compound is recrystallised from ethyl acetate (15 ml).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04243665
Source datasetuspto-grants-1981_01
ORD IDord-3465046ca378426fa6c710e55f2cf957
Source noteuspto-grants-1981_01