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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 597692Erstellt: 25. Oktober 2026

Triethylamine → 1-ethoxycarbonyloxy-6-chloro1H-benzotriazole

https://huagongshe.com/reaction/597692

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, 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04014915
Quelldatensatzuspto-grants-1977_03
ORD IDord-9d4deea5a1ce4862b6a56f488fac89a3
Quellennotizuspto-grants-1977_03