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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257132Generated: October 25, 2026

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

https://huagongshe.com/reaction/257132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3-Benzothiadiazol-7-ylmethanolHCID 20096433—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
ProductBenzo[d][1,2,3]thiadiazole-7-carbaldehydeHCID 1483568191.5%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260423
Source datasetuspto-grants-1993_11
ORD IDord-e7c17657d5874034be389a4126755d23
Source noteuspto-grants-1993_11