HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 16beta-Ethyl-17beta-(3-methylbutyryl)oxyacetoxy-4-estren-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-one | HCID 15593764 | — |
| Reactant | Sodium Isovalerate | HCID 23673832 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 16beta-Ethyl-17beta-(3-methylbutyryl)oxyacetoxy-4-estren-3-one | HCID 70467308 | 87.8% |
Reaction Steps
In a mixture of 2 ml of water and 2 ml of acetone is dissolved 0.26 g of sodium isovalerate, and 0.45 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one and 10 ml of DMF are added to the above solution. The mixture is refluxed for 6 hours, and thereafter treated in the same manner as Example 26. The reaction mixture is then subjected to column chromatography. Following passage of 100 ml of diisopropyl ether-n-hexane (2:8), elution is carried out with 400 ml of a 1:1 mixture of the same solvents. The elutate is evaporated under reduced pressure to remove the solvent, giving 0.415 g of the above-identified compound as a colorless viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04609650 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-d51e0e4020a2488db56dcccc51125eed |
| Source note | uspto-grants-1986_09 |