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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35359Generated: October 28, 2026

Chloroacetyl chloride → trans-2-chloro-N-(2,3,4,5-tetrahydro-5-hydroxy-7-methoxy-1-benzoxepin-4-yl)acetamide

https://huagongshe.com/reaction/35359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactanttrans-4-Amino-7-methoxy-2,3,4,5-tetrahydro-1-benzoxepin-5-olHCID 14256309—
SolventChloroformHCID 6212—
Producttrans-2-chloro-N-(2,3,4,5-tetrahydro-5-hydroxy-7-methoxy-1-benzoxepin-4-yl)acetamideHCID 1425631281%

Reaction Steps

A solution of 17 g of trans-4-amino-7-methoxy-2,3,4,5-tetrahydro-1-benzoxepin-5-ol dissolved in 700 ml of hydrocarbon-stabilized chloroform was treated with 16 ml of triethylamine at room temperature and 10 g of chloroacetyl chloride dissolved in 80 ml of chloroform was slowly added thereto. The reaction mixture was allowed to stand at room temperature for 24 hours and the solid removed by filtration and washed with chloroform. The filtrate was washed twice with dilute hydrochloric acid solution, followed by a wash with water and dried over anhydrous magnesium sulfate. The filtrate was evaporated to dryness and triturated with ether to yield 18.8 g of trans-2-chloro-N-(2,3,4,5-tetrahydro-5-hydroxy-7-methoxy-1-benzoxepin-4-yl)acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766212
Source datasetuspto-grants-1988_08
ORD IDord-b1eea77b75ca4e66a49e9c58bd64f7b3
Source noteuspto-grants-1988_08