Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536418Generated: October 30, 2026

(7-Bromo-benzo[1,2,5]thiadiazol-4-yl)-methanol → 7-Bromo-2,1,3-benzothiadiazole-4-carboxaldehyde

https://huagongshe.com/reaction/536418

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(7-Bromo-benzo[1,2,5]thiadiazol-4-yl)-methanolHCID 58497958—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product7-Bromo-2,1,3-benzothiadiazole-4-carboxaldehydeHCID 5849796283%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859592B2
Source datasetuspto-grants-2014_10
ORD IDord-0e8d202a695d4a0b99fb96e48552fe4c
Source noteuspto-grants-2014_10