HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,3-Benzothiadiazol-7-ylmethanol → Benzo[d][1,2,3]thiadiazole-7-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,3-Benzothiadiazol-7-ylmethanol | HCID 20096433 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Benzo[d][1,2,3]thiadiazole-7-carbaldehyde | HCID 14835681 | 91.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05260423 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-e7c17657d5874034be389a4126755d23 |
| Source note | uspto-grants-1993_11 |