HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1414912Erstellt: 26. Oktober 2026
alpha-Hydroxytriazolam → 6-(o-chlorophenyl)-8-chloro-4H-s-triazolo[4,3-a][1,4] benzodiazepine-1-carboxaldehyde
https://huagongshe.com/reaction/1414912
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | alpha-Hydroxytriazolam | HCID 1963 | — |
| Katalysator | HCID 178418406 | HCID 178418406 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 6-(o-chlorophenyl)-8-chloro-4H-s-triazolo[4,3-a][1,4] benzodiazepine-1-carboxaldehyde | HCID 21486012 | — |
Reaktionsschritte
A suspension of 1.3 g of 6-(o-chlorophenyl)-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-methanol and 3.4 g of manganese dioxide in 200 ml of benzene is refluxed for 2 hours. The reaction mixture is then filtered and the filtrate concentrated by evaporation. The resulting foam is dissolved in a little ethyl acetate and the solution chromatographed on ca. 60 g of silica gel (Merck, 0.063 - 0.2 mm particle size) with ethyl acetate as the eluant. Fractions each of ca. 80 ml are collected. The fractions 4-8 are combined, concentrated by evaporation, and the residue crystallised from an ethyl acetate/ether/petroleum ether mixture to obtain 6-(o-chlorophenyl)-8-chloro-4H-s-triazolo[4,3-a][1,4] benzodiazepine-1-carboxaldehyde, M.P. 182°-189°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04002764 |
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| Quelldatensatz | uspto-grants-1977_01 |
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| ORD ID | ord-7dd22304101e42378d97781f697d154a |
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| Quellennotiz | uspto-grants-1977_01 |
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