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Sodium Sulfate → 20-Methylpregna-5,7-diene-1alpha,3beta,21-triol

HRID 1587615
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HRID 1587615 반응식
COC([O:5][C@@H:6]1[C@@:28]2([CH3:29])[C:10](=[CH:11][CH:12]=[C:13]3[C@@H:27]2[CH2:26][CH2:25][C@@:24]2([CH3:30])[C@H:14]3[CH2:15][CH2:16][C@@H:17]2[CH:18]([C:20](OC)=[O:21])[CH3:19])[CH2:9][C@@H:8]([O:31]C(OC)=O)[CH2:7]1)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].S([O-])([O-])(=O)=O.[Na+].[Na+]>O1CCCC1.C(OCC)C>[CH3:19][CH:18]([C@@H:17]1[C@:24]2([CH3:30])[C@H:14]([C:13]3[C@H:27]([CH2:26][CH2:25]2)[C@:28]2([CH3:29])[C:10]([CH2:9][C@@H:8]([OH:31])[CH2:7][C@@H:6]2[OH:5])=[CH:11][CH:12]=3)[CH2:15][CH2:16]1)[CH2:20][OH:21]
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참가 물질

6

반응물 3

HCID 24436Sodium SulfateHCID 18652401Methyl 1alpha,3beta-bis(methoxycarbonyloxy)pregna-5,7-diene-20 carboxylateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 6778765420-Methylpregna-5,7-diene-1alpha,3beta,21-triol수율 117.3%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매
HCID 8028
Tetrahydrofuran
용매

실험 절차

Methyl 1α,3β-bis(methoxycarbonyloxy)pregna-5,7-diene-20-carboxylate (70 mg) was added to a suspension of 10 mg of lithium aluminum hydride in 5 ml of tetrahydrofuran with ice cooling and the mixture was stirred with ice cooling for 30 minutes. The resulting reaction mixture was diluted with diethyl ether and the excess reducing agent was decomposed with a saturated aqueous solution of sodium sulfate. The insoluble matter was filtered off and washed well with ethyl acetate. The filtrate and washings were combined and concentrated. The residue was washed with cold diethyl ether to give 58 mg of 20-methylpregna-5,7-diene-1α,3β,21-triol.

후처리

  1. customThe resulting reaction mixture
  2. filtrationThe insoluble matter was filtered off
  3. washwashed well with ethyl acetate
  4. concentrationconcentrated
  5. washThe residue was washed with cold diethyl ether

출처 및 근거

ORD 기록
ord-c341d2f6ddb34b81bf80f6413866c590
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05218109

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