HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → [2-(4-Chlorophenyl)thiazol-5-yl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(4-Chlorophenyl)-1,3-thiazole-5-carbaldehyde | HCID 45036822 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [2-(4-Chlorophenyl)thiazol-5-yl]methanol | HCID 59562416 | 98.3% |
Reaction Steps
To a suspension of 2-(4-chlorophenyl)thiazole-5-carbaldehyde (3.26 g, 14.6 mmol) in methanol (50 ml) is added the sodium borohydride (568 mg, 15 mmol) portionwise at room temperature. The reaction mixture is stirred at room temperature for 2 h. The reaction mixture is quenched with 50 ml of an aqueous saturated solution of ammonium chloride, extracted with dichloromethane (2×100 ml). The combined organic extracts are dried with magnesium sulphate, filtered and evaporated to dryness to give [2-(4-chlorophenyl)thiazol-5-yl]methanol (3.24 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08956999B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-31e7fe97978645ac95802f4f75d84ec1 |
| Source note | uspto-grants-2015_02 |