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HRID 2082684Erstellt: 26. Oktober 2026

Dimethylformamide → 7-Thia-2,4,5-triazatricyclo(6.4.0.0,2,6)dodeca-1(12),3,5,8,10-pentaene

https://huagongshe.com/reaction/2082684

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktHydrazinecarboxaldehydeHCID 12229—
EduktSodium hydrideHCID 24758—
Edukt1-Chloro-2-isothiocyanatobenzeneHCID 123171—
LösungsmittelWaterHCID 962—
Produkt7-Thia-2,4,5-triazatricyclo(6.4.0.0,2,6)dodeca-1(12),3,5,8,10-pentaeneHCID 254568—

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

Five grams (30.0 mmoles) of o-chlorophenylisothiocyanate were dissolved in 50 ml. of dry DMF. A solution of 1.8 g. (30.0 mmoles) of formylhydrazine in 50 ml. of dry DMF was added dropwise rapidly to the stirred reaction mixture. The temperature of the reaction rose to about 45° C. The temperature was maintained between 60° C. and 100° C. for 24 hours. Thirty millimoles, 1.5 g., of sodium hydride as a 50% mineral oil suspension was added to the reaction mixture. The reaction was completed by heating at reflux temperature (160° C) for about 185 hours. The cooled mixture was poured into water. The aqueous mixture was extracted with n-hexane to remove mineral oil. The product was extracted with ethyl acetate. The ethyl acetate extract was washed (water), dried (MgSO4) and evaporated in vacuo to a residual oil. the oil was covered with dry ether an the product crystallized upon standing. The yield of s-triazolo[3,4-b]benzothiazole, m.p. about 175°-176° C., was 200 mg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04082762
Quelldatensatzuspto-grants-1978_04
ORD IDord-23156dacf8c6489f9b9a6d11efa89586
Quellennotizuspto-grants-1978_04