HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 69946895, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 69740094 | HCID 69740094 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69946895 | HCID 69946895 | 50% |
Reaction Steps
Sodium borohydride (27 mg, 0.708 mmol) was added to a magnetically stirred solution of trans-2-carboethoxy-5-acetoxy-1,3-oxathiolane (52 mg, 0.236 mmol) in methanol (1 mL) at 0° C. under an argon atmosphere. The resultant solution was stirred for 25 minutes at 0° C. The reaction was quenched with 2 drops of saturated ammonium chloride solution followed by dilution with diethyl ether (4 mL). This mixture was stirred at room temperature for 15 minutes and then was dried over anhydrous magnesium sulphate. The drying agent was removed by suction filtration and the filtrate was concentrated under reduced pressure. The crude product obtained was subjected to column chromatography (50% EtOAc-hexane) to afford 21 mg (50%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06175008B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-fb6662a38e2f4cc3bbdeb821a6635cfa |
| Source note | uspto-grants-2001_01 |