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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1578216Erstellt: 26. Oktober 2026

Triethylamine → 1-ethoxycarbonyloxy-6-chloro1H-benzotriazole

https://huagongshe.com/reaction/1578216

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
Edukt6-Chloro-1-hydroxy-1H-benzotriazoleHCID 232711—
LösungsmittelBenzeneHCID 241—
Produkt1-ethoxycarbonyloxy-6-chloro1H-benzotriazoleHCID 1329285345,7%

Reaktionsschritte

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-chloro1H-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, 1 N 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE030752
Quelldatensatzuspto-grants-1981_09
ORD IDord-2df67708dc2243a6b5cf0abe2102c9f5
Quellennotizuspto-grants-1981_09