HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-[2-(4-Chlorophenyl)thiazol-5-yl]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-[2-(4-Chlorophenyl)-1,3-thiazol-5-yl]-1-ethanone | HCID 7062288 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[2-(4-Chlorophenyl)thiazol-5-yl]ethanol | HCID 59562475 | 96.9% |
Reaction Steps
To a suspension of 1-[2-(4-chloro-phenyl)-thiazol-5-yl]ethanone (5 g, 21 mmol) in methanol (100 ml) is added sodium borohydride (832 mg, 22 mmol) at room temperature. The reaction mixture is stirred at room temperature for 0.5 hour. The reaction mixture is quenched with 100 ml of an aqueous saturated solution of ammonium chloride, extracted with dichloromethane (2×150 ml). The combined organic extracts are dried over magnesium sulphate, filtered and evaporated to dryness to give 1-[2-(4-chloro-phenyl)-thiazol-5-yl]ethanol (4.88 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530667B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-9c642914da4d4470aa47031ae72f88b8 |
| Source note | uspto-grants-2013_09 |