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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505242Generated: November 3, 2026

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

https://huagongshe.com/reaction/1505242

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 (Example 5.2) (20.22 g) 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 numberUS09216973B2
Source datasetuspto-grants-2015_12
ORD IDord-3b53fb16fb384addbdd88e5d3602d48d
Source noteuspto-grants-2015_12