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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156035Generated: October 25, 2026

Acetyl chloride → Acetamide, N-(4-((1-methyl-4-phenyl-4-piperidinyl)oxy)phenyl)-

https://huagongshe.com/reaction/1156035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantPiperidine, 4-(p-aminophenoxy)-1-methyl-4-phenyl-HCID 3060392—
SolventBenzeneHCID 241—
ProductAcetamide, N-(4-((1-methyl-4-phenyl-4-piperidinyl)oxy)phenyl)-HCID 3060397—

Reaction Steps

A solution of 0.85 g of acetyl chloride in 5 ml of benzene is added dropwise to a solution of 2.8 g of 4-(4-aminophenoxy)-1-methyl-4-phenylpiperidine and 1.1 g of triethylamine in 10 ml of benzene. After stirring the mixture at room temperature for 6 hours, it is concentrated; the resulting residue is taken up with 30 ml each of water and diethyl ether; the obtained mixture is shaken thoroughly, and the organic phase is separated off, dried over sodium sulfate and concentrated. 2.8 g of the title compound remain as a viscous yellow oil which crystallizes (m.p. 143° to 144° C.) from diethylether after standing for several days.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04333942
Source datasetuspto-grants-1982_06
ORD IDord-870e1b1a003c4c58bf0b300d6fd1bbc5
Source noteuspto-grants-1982_06