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-chlorophenyl)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 1 hour. The reaction mixture is quenched with saturated aqueous ammonium chloride solution (100 ml) and extracted with dichloromethane (2×150 ml). The combined organic extracts are dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to give 1-[2-(4-chlorophenyl)thiazol-5-yl]ethanol (4.88 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541594B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-0fb724ba2dbf442d8e495a8f331d6d73 |
| Source note | uspto-grants-2013_09 |