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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257132Erstellt: 26. Oktober 2026

1,2,3-Benzothiadiazol-7-ylmethanol → Benzo[d][1,2,3]thiadiazole-7-carbaldehyde

https://huagongshe.com/reaction/257132

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2,3-Benzothiadiazol-7-ylmethanolHCID 20096433—
KatalysatorHCID 178418406HCID 178418406—
LösungsmittelChloroformHCID 6212—
ProduktBenzo[d][1,2,3]thiadiazole-7-carbaldehydeHCID 1483568191,5%

Reaktionsschritte

To a solution of 16.6 g of 7-hydroxymethylbenzo-1,2,3-thiadiazole in 100 ml of chloroform there are introduced with stirring at room temperature 35 g of manganese dioxide, during which process the internal temperature rises briefly to 31° C. When the temperature has dropped again to 25° C., the mixture is heated and refluxed overnight. Another 5 g of manganese dioxide are subsequently added, and heating of the mixture is continued until the reaction is complete. The hot mixture is filtered over Hyflo and the filtrate is then evaporated. The residue is digested in a little hexane and then filtered, which gives 15 g (91.4%) of the title compound of m.p. 134°-136° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05260423
Quelldatensatzuspto-grants-1993_11
ORD IDord-e7c17657d5874034be389a4126755d23
Quellennotizuspto-grants-1993_11