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HRID 64712作成日:2026年10月26日

2-Ethylbutyric acid → 16beta-Ethyl-17beta-(2-ethylbutyryl)oxyacetoxy-4-estren-3-one

https://huagongshe.com/reaction/64712

反応式

関与物質

役割名称HCID仕込み量
反応物2-Ethylbutyric acidHCID 6915—
反応物16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
溶媒AcetoneHCID 180—
溶媒Sodium HydroxideHCID 14798—
生成物16beta-Ethyl-17beta-(2-ethylbutyryl)oxyacetoxy-4-estren-3-oneHCID 70466967—

反応手順

In 35 ml of acetone is dissolved 1.0 ml of 2-ethylbutyric acid, and 4.6 ml of 2N-NaOH and then 1.9 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one are added to the above solution. The mixture is refluxed for 3 hours. The acetone is distilled off under reduced pressure and the residue is extracted with two 100 ml portions of ethyl acetate. The organic layers are combined, washed with water and saturated aqueous sodium chloride 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 50 ml of ether, elution is carried out with 300 ml of the same solvent. The eluate is evaporated under reduced pressure to remove the solvent, giving 1.63 g of the above-identified compound as a light-yellow viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04609650
出典データセットuspto-grants-1986_09
ORD IDord-685484c6284b41cb99dbeb91de9c8807
出典メモuspto-grants-1986_09