HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536417Generated: October 30, 2026
Potassium Carbonate → (7-Bromo-benzo[1,2,5]thiadiazol-4-yl)-methanol
https://huagongshe.com/reaction/536417
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-7-bromomethyl-benzo[1,2,5]thiadiazole | HCID 11415578 | — |
| Solvent | Water | HCID 962 | — |
| Product | (7-Bromo-benzo[1,2,5]thiadiazol-4-yl)-methanol | HCID 58497958 | 87.5% |
Reaction Steps
A mixture of 4-bromo-7-bromomethyl-benzo[1,2,5]thiadiazole (29.05 g) (Example II), 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08859592B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-7ee9b8c01d1c4e54bee0cfdf34c0c103 |
|---|
| Source note | uspto-grants-2014_10 |
|---|