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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866850Generated: October 26, 2026

Chloroacetyl chloride → N-(4-chlorophenacyl) chloroacetamide

https://huagongshe.com/reaction/866850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-1-(4-chlorophenyl)ethan-1-one hydrochlorideHCID 2798211—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductN-(4-chlorophenacyl) chloroacetamideHCID 5368537757.3%

Reaction Steps

To a well stirred suspension of 20.6 g of 4-chlorophenacylamine hydrochloride in 70 ml of benzene and 70 ml of water which was cooled to below 7° C were added simultaneously 110 ml of 2N NaOH solution and 12.4 g of chloroacetyl chloride dissolved in 30 ml of benzene. After the addition was complete, the reaction mixture was warmed to room temperature and stirred at room temperature for 3 hours. At the end of this period, the formed precipitate was filtered, and the benzene layer was separated. The aqueous layer was extracted twice with 50 ml of benzene. The combined benzene layer was dried over anhydrous sodium sulfate, and evaporated to dryness. The residue together with the precipitate obtained above was combined and recrystallized from ethanol to give 14.1 g (57 percent) of N-(4-chlorophenacyl) chloroacetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101660
Source datasetuspto-grants-1978_07
ORD IDord-83d612f9492a4e9883641d30e30df7d7
Source noteuspto-grants-1978_07