HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 597692Erstellt: 25. Oktober 2026
Triethylamine → 1-ethoxycarbonyloxy-6-chloro1H-benzotriazole
https://huagongshe.com/reaction/597692
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | 6-Chloro-1-hydroxy-1H-benzotriazole | HCID 232711 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 1-ethoxycarbonyloxy-6-chloro1H-benzotriazole | HCID 13292853 | 45,7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04014915 |
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| Quelldatensatz | uspto-grants-1977_03 |
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| ORD ID | ord-9d4deea5a1ce4862b6a56f488fac89a3 |
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| Quellennotiz | uspto-grants-1977_03 |
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