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 | 96.8% |
Reaction Steps
To a stirred solution of 1-[2-(4-chlorophenyl)thiazol-5-yl]ethanone (2.38 g, 10 mmol) in methanol (20 ml) at 0° C. is added sodium borohydride (379 mg, 10.5 mmol) in one portion. The resultant solution is allowed to warm to room temperature, and is then stirred at room temperature for 3 hours. The reaction is quenched with saturated aqueous ammonium chloride solution (200 ml) and extracted with chloroform (200 ml). The organic layer is dried over anhydrous magnesium sulfate and concentrated in vacuuo to give desired product as a brown solid (2.32 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08956999B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-0ba5604d72534a50bf49f6905b656d5f |
| Source note | uspto-grants-2015_02 |