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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082995Generated: October 25, 2026

Triethylamine → 1-ethoxycarbonyloxy-6-chloro1H-benzotriazole

https://huagongshe.com/reaction/2082995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant6-Chloro-1-hydroxy-1H-benzotriazoleHCID 232711—
SolventBenzeneHCID 241—
Product1-ethoxycarbonyloxy-6-chloro1H-benzotriazoleHCID 1329285345.7%

Reaction Steps

A solution of ethyl chloroformate (2.17 g.) in benzene (10 ml.) was added dropwise to a solution of 1-hydroxy-6-chloro-1H-benzotriazole (3.38 g.) and triethylamine (2.80 ml.) in benzene (30 ml.) under ice-cooling and stirring. Benzene (30 ml.) was further added to the mixture and the reaction temperature was slowly elevated to room temperature. The mixture was allowed to stand overnight. Precipitated crystals were filtered off and the filtrate was concentrated. Benzene was added to the residue and an insoluble material was filtered off. The filtrate was concentrated to give 1-ethoxycarbonyloxy-6-chloro-1H-benzotriazole (2.2 g.), crystals. The precipitated crystals filtered off and the insoluble material in benzene were mixed and then washed with water, a sodium bicarbonate aqueous solution, 1N hydrochloric acid and water, and recrystallized from methanol (75 ml.) to give the desired compound (3.5 g.), white needles, mp 160° to 162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04083848
Source datasetuspto-grants-1978_04
ORD IDord-752968fc83c340698b0c3ba7a06b828f
Source noteuspto-grants-1978_04