HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Cholest-4-en-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Cholesterol | HCID 5997 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Aluminum isopropoxide | HCID 11143 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Cholest-4-en-3-one | HCID 91477 | — |
Reaction Steps
111 g. of 3β-hydroxy-5-cholestene is heated in 2.2 l. of toluene and 111 ml. of cyclohexane to boiling. A solution of 55.5 g. of aluminum isopropylate in 666 ml. of toluene is added dropwise thereto. The mixture is then further heated for 90 minutes with gradual distillation. The cooled reaction solution is diluted with ether, washed with dilute sulfuric acid and water, and concentrated. The residue is distilled with steam and the crude product, obtained after extraction with methylene chloride, is chromatographed on silica gel. After recrystallization from methanol, 70 g. of 4-cholesten-3-one is obtained, m.p. 79° - 80.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04100026 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-3ae943e8573c47a38c4ad419ccde1980 |
| Source note | uspto-grants-1978_07 |