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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086030Generated: November 1, 2026

2-Chloroacetophenone → 4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(2-oxo-2-phenyl-ethoxy)-benzamide

https://huagongshe.com/reaction/1086030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroacetophenoneHCID 10757—
ReactantSodium hydrideHCID 24758—
Reactant4-amino-5-chloro-N-(2-(diethylamino)ethyl)-2-hydroxybenzamide hydrochlorideHCID 14116877—
SolventDimethylformamideHCID 6228—
Product4-Amino-5-chloro-N-(2-diethylamino-ethyl)-2-(2-oxo-2-phenyl-ethoxy)-benzamideHCID 1411689050.1%

Reaction Steps

To a stirred suspension of sodium hydride (320 mg of 60%, 8 mmoles, washed with n-pentane) in DMF (15 ml) was added 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide hydrochloride (1.289 g, 4 mmoles) and the mixture stirred for 20 minutes followed by addition of chloroacetophenone (619 mg, 4 mmoles). The mixture was stirred 4 hours, poured into ice-cold water (50 ml) whereupon a solid separated out. This was isolated by filtration, dried and recrystallized from methanol to give 810 mg (50%) of the title compound as white solid mp 153°-4°. The NMR spectrum (90 MHz) in CDCl3 gave the following resonances: δ 8.64 (bs, 1H); 8.2 (s, 1H); 8 (m, 2H); 7.6 (m, 3H); 6.22 (s, 1H); 5.36 (s, 2H); 4.4 (s, 2H); 3.52 (m, 2H); 2.64 (m, 6H); 1.01 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011992
Source datasetuspto-grants-1991_04
ORD IDord-0a2c655b57ab41d7a4a84f2a07afb99b
Source noteuspto-grants-1991_04