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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129048Generated: October 31, 2026

p-Anisoyl chloride → N,N-Diethyl-para-anisamide

https://huagongshe.com/reaction/129048

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantDiethylamineHCID 8021—
ReactantTriethylamineHCID 8471—
SolventDichloromethaneHCID 6344—
ProductN,N-Diethyl-para-anisamideHCID 231459—

Reaction Steps

To a mixture of diethylamine (89.1 mL), triethylamine (120.2 mL) and CH2Cl2 (500 mL) cooled in an ice-bath was added dropwine p-anisoyl chloride (133.8 g) over 40 minutes. The reaction mixture was stirred at room temperature for 40 minutes, the mixture was filtered, washed with ether and the solvent was removed in vacuo. Ether was added, then water to the residue, then the organic layer was separate and washed with 5% NaoH, then in HCl, then brine and then was dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by kugelrohr distillation at 140°-180° C. under high vacuum to afford 163.8 g of 4-methoxy-N,N-diethylbenzamide, m.p. 40°-42° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466701
Source datasetuspto-grants-1995_11
ORD IDord-3ff1f62639f54f09bf57bbb085481bc0
Source noteuspto-grants-1995_11