HuagongsheHuagongshe Chemistry Print Report · For research reference only
(7-Bromo-benzo[1,2,5]thiadiazol-4-yl)-methanol → 7-Bromo-2,1,3-benzothiadiazole-4-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (7-Bromo-benzo[1,2,5]thiadiazol-4-yl)-methanol | HCID 58497958 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Bromo-2,1,3-benzothiadiazole-4-carboxaldehyde | HCID 58497962 | 83% |
Reaction Steps
To a solution of (7-bromo-benzo[1,2,5]thiadiazol-4-yl)-methanol (20.22 g) (Example I2) in dichloromethane (185 ml) was added manganese(IV) oxide (71.7 g). The suspension was stirred at ambient temperature for 16 hours. The reaction mixture was filtered through a plug of Celite®. The filtrate was concentrated to give 7-bromo-benzo[1,2,5]thiadiazole-4-carbaldehyde (16.65 g) as an orange solid. 1H-NMR (400 MHz, CDCl3): 10.74 (s, 1H), 8.11-8.05 (m, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859592B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-0e8d202a695d4a0b99fb96e48552fe4c |
| Source note | uspto-grants-2014_10 |