HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 10740169, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | HCID 70045315 | HCID 70045315 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10740169 | HCID 10740169 | 96.2% |
Reaction Steps
To a solution of 13.86 g of 3β-acetoxy-21-nitro-5β-pregn-20-en-14β-ol (Eberlein W. et al., Chem. Ber., 1974, 107, 1275) in 440 ml of diethyl ether and 440 ml of ethanol, 2.86 g NaBH4 were added at room temperature. After 1 hr. the mixture was neutralized with aqueous sodium dihydrogenphosphate and extracted with methylene chloride. The organic layer was washed with water, dried over anhydrous sodium sulfate and evaporated to dryness to give 13.40 g of 3β-acetoxy-21-nitro-5β-pregnane-14β-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05583127 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-625b732f5f044ad28e1579a0c547ec43 |
| Source note | uspto-grants-1996_12 |