HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64724Generated: October 25, 2026
N,N-Dimethylaniline → 16beta-Ethyl-17beta-(2-methylvaleryl)oxyacetoxy-4-estren-3-one
https://huagongshe.com/reaction/64724
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 2-Methylvaleryl chloride | HCID 107385 | — |
| Reactant | 16beta-Ethyl-17beta-glycoloyloxy-4-estren-3-one | HCID 70466441 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 16beta-Ethyl-17beta-(2-methylvaleryl)oxyacetoxy-4-estren-3-one | HCID 70466930 | 19.8% |
Reaction Steps
In 20 ml of dichloromethane are dissolved 0.5 g of 16β-ethyl-17β-glycoloyloxy-4-estren-3-one and 0.2 ml of N,N-dimethylaniline, and 0.5 g of 2-methylvaleryl chloride is added to the above solution. The mixture is refluxed for 6 hours. After cooling, the reaction mixture is diluted with 150 ml of ethyl acetate and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 200 ml of diisopropyl ether-n-hexane (2:8), elution is carried out with 500 ml of a 1:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 0.126 g of the above-identified compound as a light-yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04609650 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-6c373de8ad0a482ca08749a90e9f07a1 |
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| Source note | uspto-grants-1986_09 |
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