HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618090Generated: November 1, 2026
Potassium Carbonate → HCID 66702981, compound
https://huagongshe.com/reaction/1618090
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Bromomethyl)-4-(trifluoromethyl)benzene | HCID 123062 | — |
| Reactant | 2-Cyano-6-hydroxybenzothiazole | HCID 9881912 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 66702981 | HCID 66702981 | 89.5% |
Reaction Steps
A suspension of 2-cyano-6-hydroxybenzothiazole (1.0 g, 5.68 mmol) in acetone (5 mL) was prepared in a 100-mL 2-necked round-bottomed flask fitted with a reflux condenser. Anhydrous potassium carbonate (0.94 g, 6.82 mmol) was added to the reaction mixture and the suspension turned to a yellow solution. Then 4-(trifluoromethyl)benzyl bromide (1.49 g, 6.25 mmol) was added and the reaction mixture was heated at reflux for 15 h using a heated stir plate and oil bath. The reaction mixture was allowed to cool to ambient temperature and then filtered to remove inorganic salts. The filtrate was concentrated by rotoevaporation to provide 1.7 g (89% yield) of an off-white solid that was used without purification. The structure was confirmed by 1H NMR analysis in DMSO-d6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765969B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-8abcc56255174c11b9f60ac35cdca108 |
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| Source note | uspto-grants-2014_07 |
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