HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 69762612, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22809505 | HCID 22809505 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 69762612 | HCID 69762612 | 76.6% |
Reaction Steps
To the solution of 3α,6α-dihydroxy-5β-cholestan-24-one (2.6 g) in methanol (200 ml) was added sodium borohydride (2 g) and stirred for one hour under cooling with ice. After decomposition of excess sodium borohydride with aqueous solution of acetic acid, the mixture was evaporated to reduce the volume to about 100 ml and the residue was extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over magnesium sulfate and evaporated to give 2.0 g of 3α,6α,24-trihydroxy-5β-cholestane having a melting point of 169°-173° C. after recrystallization from chloroform.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04179452 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-e814d2770dd64bf589673b56e027d362 |
| Source note | uspto-grants-1979_12 |