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1beta,2beta-Methylene-5-androstene-3beta,17beta-diol → 1beta,2beta-Methylene-4-androstene-3,17-dione

HRID 371846
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HRID 371846 반응식
[CH2:1]1[C@@H:3]2[C@H:4]([OH:22])[CH2:5][C:6]3[C@:19]([CH3:20])([C@H:2]12)[C@@H:18]1[C@H:9]([C@H:10]2[C@@:14]([CH2:16][CH2:17]1)([CH3:15])[C@@H:13]([OH:21])[CH2:12][CH2:11]2)[CH2:8][CH:7]=3.CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O>CC(C)=O>[CH2:1]1[C@@H:3]2[C:4](=[O:22])[CH:5]=[C:6]3[C@:19]([CH3:20])([C@H:2]12)[C@@H:18]1[C@H:9]([C@H:10]2[C@@:14]([CH2:16][CH2:17]1)([CH3:15])[C:13](=[O:21])[CH2:12][CH2:11]2)[CH2:8][CH2:7]3
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 566286851beta,2beta-Methylene-5-androstene-3beta,17beta-diolHCID 131709961Jones' reagent

생성물 1

HCID 542623781beta,2beta-Methylene-4-androstene-3,17-dione

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

The 1β,2β-methylene-5-androstene-3β,17β-diol is dissolved in acetone and Jones reagent added until a persistent yellow-orange color appears. After stirring at room temperature for ten minutes the mixture is poured onto ice-water and the precipitate is collected by filtration. The precipitate is dissolved in a solution of sodium methoxide in methanol and stirred for a period of 30 minutes at room temperature. The methanol is removed and the residue triturated with water. The solid which results is filtered and crystallized from acetone to yield 1β,2β-methylene-4-androstene-3,17-dione.

후처리

  1. additionis poured onto ice-water
  2. filtrationthe precipitate is collected by filtration
  3. dissolutionThe precipitate is dissolved in a solution of sodium methoxide in methanol
  4. stirringstirred for a period of 30 minutes at room temperature
  5. customThe methanol is removed
  6. customthe residue triturated with water
  7. customThe solid which results
  8. filtrationis filtered
  9. customcrystallized from acetone

출처 및 근거

ORD 기록
ord-418bc839e03d4f55af1df74410c7c3b8
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04087524

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