HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 19744741, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | HCID 86747107 | HCID 86747107 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19744741 | HCID 19744741 | 97% |
Reaction Steps
150 mg of ethyl (E)-5-styryloxazole-2carboxylate Yakugaku Zasshi, vol. 91, page 425 (1971)) was suspended in 15 ml of ethanol, and at -10° C., 5 ml of an ethanol solution of 35 mg of sodium borohydride and 123 mg of calcium chloride was added, and the mixture was stirred at room temperature for 3 hours. The reaction mixture was concentrated under reduced pressure, and water and ethyl ether were added to the residue to perform extraction. The organic layer was separated, and then dried over anhydrous magnesium sulfate. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure to give 120 mg (yield 97%) of the captioned compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05234946 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-ed2dd84bb08549fc9a3e6af90a72a7d4 |
| Source note | uspto-grants-1993_08 |