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HRID 64733생성일: 2026년 10월 24일

Dimethylformamide → 16beta-Ethyl-17beta-(3,3-dimethylbutyryl)oxyacetoxy-4-estren-3-one

https://huagongshe.com/ko/reaction/64733

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물tert-Butylacetic acidHCID 14057—
반응물Sodium HydroxideHCID 14798—
반응물16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
용매AcetoneHCID 180—
생성물16beta-Ethyl-17beta-(3,3-dimethylbutyryl)oxyacetoxy-4-estren-3-oneHCID 7046727261%

반응 단계

In 10 ml of acetone is dissolved 1.16 g of 3,3-dimethylbutyric acid, and 5.0 ml of 2N-NaOH is added, followed by addition of 1.15 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one and 20 ml of DMF. The mixture is refluxed for 5 hours, and thereafter treated in the same manner as Example 26. The reaction mixture is chromatographed on a silica gel column. Following passage of 200 ml of n-hexanediisopropyl ether (3:7), elution is carried out with a 1:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 0.76 g of the above-identified compound as a colorless viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04609650
출처 데이터셋uspto-grants-1986_09
ORD IDord-fc603816905c42dc89c27894771d8e96
출처 메모uspto-grants-1986_09