(1alpha,3beta)-1,3-Bis (acetyloxy)androsta-5,7-dien-17-one → (1alpha,3beta)-1,3-Dihydroxyandrosta-5,7-dien-17-one

HRID 481809

反応式

HRID 481809 の反応式
C([O:4][C@@H:5]1[C@@:22]2([CH3:23])[C:9](=[CH:10][CH:11]=[C:12]3[C@@H:21]2[CH2:20][CH2:19][C@@:17]2([CH3:18])[C@H:13]3[CH2:14][CH2:15][C:16]2=[O:24])[CH2:8][C@@H:7]([O:25]C(=O)C)[CH2:6]1)(=O)C.C[O-].[Na+]>CO>[OH:4][C@@H:5]1[C@@:22]2([CH3:23])[C:9](=[CH:10][CH:11]=[C:12]3[C@@H:21]2[CH2:20][CH2:19][C@@:17]2([CH3:18])[C@H:13]3[CH2:14][CH2:15][C:16]2=[O:24])[CH2:8][C@@H:7]([OH:25])[CH2:6]1

参加物

4

実験手順

A 3-L three-necked flask equipped with a mechanical stirrer was charged with 114.5 g (296 mmol) of (1α,3β)-1,3-bis (acetyloxy)androsta-5,7-dien-17-one, a known compound, 586 mL of methanol, and 29 mL of 25% sodium methoxide in methanol. After stirring at room temperature for 20 hr, the reaction was quenched by the addition of 7.4 mL of acetic acid. Then, 880 mL of water was added dropwise over 1 h, and the mixture was stirred for another hour and then stored in a refrigerator overnight. The precipitate was filtered and washed with 3×200 mL of methanol:water (1:2). The brown solid was dried by suction for 1 hr and then under high vacuum to afford 60.1 g of (1α,3β)-1,3-dihydroxyandrosta-5,7-dien-17-one.

後処理

  1. customA 3-L three-necked flask equipped with a mechanical stirrer
  2. customthe reaction was quenched by the addition of 7.4 mL of acetic acid
  3. additionThen, 880 mL of water was added dropwise over 1 h
  4. stirringthe mixture was stirred for another hour
  5. customstored in a refrigerator overnight
  6. filtrationThe precipitate was filtered
  7. washwashed with 3×200 mL of methanol:water (1:2)
  8. customThe brown solid was dried by suction for 1 hr

出典と根拠

ORDレコード
ord-fcf117be00024be1839d62a31b0dc643
出典データセット
uspto-grants-1998_08
特許番号
US05789607

関連ノート

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