HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 3,3-Ethylenedioxy-1-methyl-5alpha-androstan-17-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 13020861 | HCID 13020861 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,3-Ethylenedioxy-1-methyl-5alpha-androstan-17-one | HCID 70360264 | 94% |
Reaction Steps
23 g of 3,3-ethylenedioxy-1α-methyl-5α-androstan-17β-ol is agitated for 1 hour at room temperature in 230 ml of dichloromethane with 20 g of pyridinium chlorochromate in the presence of 20 g of sodium acetate. The reaction solution is then diluted with ether, filtered off from the insoluble proportions, and the filtrate is washed with water. After drying and evaporation, 21.5 g of 3,3-ethylenedioxy-1-methyl-5α-androstan-17-one is obtained as the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04892867 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-39b35abbc3e243eca068c9e48bc9456d |
| Source note | uspto-grants-1990_01 |