HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 12953373, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20505778 | HCID 20505778 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12953373 | HCID 12953373 | 40% |
Reaction Steps
To a mixture of 8.0 g (0.034 mol) of ethyl, 2-chloro-4-isopropyl-5-thiazolecarboxylate and 20 ml of ethanol was added 1.3 g (0.034 mol) of sodium borohydride in 10 minutes. The reaction mixture was stirred at room temperature for 30 minutes and concentrated under reduced pressure. The residue was chromatographed on 250 g of silica gel using ether petroleum ether (1:9, v/v) as eluant. The first fraction (2.2 g) was recovered starting material. The second fraction (3.4 g) was Kugelrohr distilled at 0.5 mm (pot temperature 95° C.) go give 2.7 g (40%) of 2-chloro-4-isopropyl-5-thiazolemethanol as a colorless liquid, nD25 1.5425.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04377693 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-f1eb657974084f5cb1172390815439b0 |
| Source note | uspto-grants-1983_03 |