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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227004Generated: October 30, 2026

Acetyl chloride → Acetamide, N-(4-(diethylamino)phenyl)- (9CI)

https://huagongshe.com/reaction/2227004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant1,4-Benzenediamine, N1,N1-diethyl-, hydrochloride (1:1)HCID 75145—
SolventDichloromethaneHCID 6344—
ProductAcetamide, N-(4-(diethylamino)phenyl)- (9CI)HCID 2140080%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (22.3 g, 30.6 mL, 0.22 mol) was added to a suspension of N,N-diethyl-p-phenylenediamine hydrochloride (20 g, 0.1 mol) in dichloromethane (150 mL) at room temperature. The mixture was cooled to 0° C. and acetyl chloride (7.85 g, 0.1 mol) was added dropwise, with stirring. The mixture was allowed to warm to room temperature, and the precipitate which had formed was removed by filtration. The solid residue was washed with dichloromethane, and the combined dichloromethane solutions were concentrated. The dark oil produced was triturated with hexanes (100 mL) to afford a light brown crystalline solid, which was purified by recrystallization from 50% aqueous ethanol to afford the N-acetyl-4-diethylaminoaniline (16.5 g, 80% yield) as a gray solid. The structure of this compound was confirmed by mass spectroscopy and by 1H NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350870
Source datasetuspto-grants-1994_09
ORD IDord-f6d0dffc59144a58a215e4ab49999bda
Source noteuspto-grants-1994_09