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Potassium Bicarbonate → 21-Chloro-17-hydroxy-4-pregnene-3,20-dione

HRID 247537
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HRID 247537 반응식
[Cl:1][CH2:2][C:3](=[O:27])[C@:4]1([O:24]C=O)[C@:21]2([CH3:22])[C@H:7]([C@H:8]3[C@H:18]([CH2:19][CH2:20]2)[C@:16]2([CH3:17])[C:11](=[CH:12][C:13](=[O:23])[CH2:14][CH2:15]2)[CH2:10][CH2:9]3)[CH2:6][CH2:5]1.C(=O)(O)[O-].[K+]>CO.O>[Cl:1][CH2:2][C:3](=[O:27])[C@:4]1([OH:24])[C@:21]2([CH3:22])[C@H:7]([C@H:8]3[C@H:18]([CH2:19][CH2:20]2)[C@:16]2([CH3:17])[C:11](=[CH:12][C:13](=[O:23])[CH2:14][CH2:15]2)[CH2:10][CH2:9]3)[CH2:6][CH2:5]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 516893Potassium BicarbonateHCID 1360479021-Chloro-17-formyloxy-4-pregnene-3,20-dione

생성물 1

HCID 1013341321-Chloro-17-hydroxy-4-pregnene-3,20-dione수율 87.5%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

At room temperature, 1.6 g of 21-chloro-17-formyloxy-4-pregnene-3,20-dione is stirred in a mixture of 60 ml of methanol and 9 ml of water with 500 mg of potassium bicarbonate. After one hour, the reaction mixture is stirred into ice water. The thus-precipitated product is suctioned off, washed with water, and dried over sodium sulfate, yielding 1.3 g of 21-chloro-17-hydroxy-4-pregnene-3,20-dione; mp 239.4° C.

후처리

  1. washwashed with water
  2. dry with materialdried over sodium sulfate

출처 및 근거

ORD 기록
ord-30d909894f6f48bebbf10476f03bbbe2
출처 데이터셋
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04708823

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