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19-Trimethylsiloxy-5alpha-androstane-3beta,17beta-diol → 19-Trimethylsiloxy-5alpha-androstane-3,17-dione

HRID 1834970
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HRID 1834970 반응식
[CH3:1][Si:2]([CH3:26])([CH3:25])[O:3][CH2:4][C@@:5]12[C@@H:22]3[C@H:13]([C@H:14]4[C@@:18]([CH2:20][CH2:21]3)([CH3:19])[C@@H:17]([OH:23])[CH2:16][CH2:15]4)[CH2:12][CH2:11][C@H:10]1[CH2:9][C@@H:8]([OH:24])[CH2:7][CH2:6]2.CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O>CC(C)=O>[CH3:25][Si:2]([CH3:1])([CH3:26])[O:3][CH2:4][C@@:5]12[C@@H:22]3[C@H:13]([C@H:14]4[C@@:18]([CH2:20][CH2:21]3)([CH3:19])[C:17](=[O:23])[CH2:16][CH2:15]4)[CH2:12][CH2:11][C@H:10]1[CH2:9][C:8](=[O:24])[CH2:7][CH2:6]2
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참가 물질

4

반응물 2

HCID 2280149619-Trimethylsiloxy-5alpha-androstane-3beta,17beta-diolHCID 131709961Jones' reagent

생성물 1

HCID 2280152719-Trimethylsiloxy-5alpha-androstane-3,17-dione

시약·촉매·용매 1

HCID 180Acetone용매2회

반응 조건

온도
10 °C

실험 절차

19-Trimethylsiloxy-5α-androstane-3β,17β-diol is dissolved in acetone and chilled to 10° C. Jones reagent is added with stirring over a period of 5 minutes and the mixture left standing for an additional 20 minutes. The acetone layer is poured onto water with vigorous stirring. The solid which forms is collected by filtration, air dried and crystallized from an acetone-hexane solution to yield 19-trimethylsiloxy-5α-androstane-3,17-dione.

후처리

  1. waitthe mixture left
  2. waitstanding for an additional 20 minutes
  3. filtrationThe solid which forms is collected by filtration, air
  4. customdried
  5. customcrystallized from an acetone-hexane solution

출처 및 근거

ORD 기록
ord-888799ce0873422a860e6f2f9ac77d9a
출처 데이터셋
uspto-grants-1978_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04071625

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