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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505241Generated: November 2, 2026

Potassium Carbonate → (7-Bromo-benzo[1,2,5]thiadiazol-4-yl)-methanol

https://huagongshe.com/reaction/1505241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-7-bromomethyl-benzo[1,2,5]thiadiazoleHCID 11415578—
SolventWaterHCID 962—
Product(7-Bromo-benzo[1,2,5]thiadiazol-4-yl)-methanolHCID 5849795887.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 4-bromo-7-bromomethyl-benzo[1,2,5]thiadiazole (Example 5.1) (29.05 g), potassium carbonate (65.2 g) and water (400 ml) was stirred at 110° C. for 16 hours. The reaction mixture was cooled to ambient temperature and quenched by addition of aqueous hydrochloric acid (2M) (400 ml). Ethyl acetate (600 ml) was added to the mixture. The phases were separated and the organic layer was washed successively with aqueous hydrochloric acid (2M) (400 ml), water (250 ml) and brine (250 ml), dried over sodium sulfate and concentrated to give (7-bromo-benzo[1,2,5]thiadiazol-4-yl)-methanol (20.22 g) as a orange solid. 1H-NMR (400 MHz, CDCl3): 7.87 (d, 1H), 7.57 (d, 1H), 5.14 (s, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216973B2
Source datasetuspto-grants-2015_12
ORD IDord-c3129e3e1d6c48908bd01fa54df78f60
Source noteuspto-grants-2015_12