反応式
[CH3:1][C@@:2]12[C:10](=[O:11])[CH2:9][CH2:8][C@H:7]1[C@@H:6]1[CH2:12][CH:13]=[C:14]3[CH2:19][C@@H:18]([OH:20])[CH2:17][C@H:16]([OH:21])[C@:15]3([CH3:22])[C@H:5]1[CH2:4][CH2:3]2.C(N([CH2:28][CH3:29])CC)C.[CH2:30]([Si:32]([CH2:36][CH3:37])([CH2:34][CH3:35])Cl)[CH3:31].O>N1C=CC=CC=1>[CH2:30]([Si:32]([CH2:28][CH3:29])([CH2:34][CH3:35])[O:21][C@@H:16]1[C@@:15]2([CH3:22])[C:14](=[CH:13][CH2:12][C@@H:6]3[C@@H:5]2[CH2:4][CH2:3][C@@:2]2([CH3:1])[C@H:7]3[CH2:8][CH2:9][C:10]2=[O:11])[CH2:19][C@@H:18]([O:20][Si:32]([CH2:36][CH3:37])([CH2:34][CH3:35])[CH2:30][CH3:31])[CH2:17]1)[CH3:31]参加物
実験手順
In 600 ml of pyridine, 9.13 g of 1α-hydroxydehydroepiandrosterone was suspended. Under an argon stream, 100 ml of triethylamine and 39.0 g of triethyl chlorosilane were added to the suspension, and the mixture was stirred for 24 hours at room temperature. After adding 500 ml of water, the solvent was distilled off under vacuum. The residue was subjected to extraction with benzene. The benzene layer was successively washed with an aqueous solution of 0.5N HCl, water, saturated sodium hydrogencarbonate and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. The residue obtained by distilling off the solvent under vacuum was subjected to silica gel column chromatography and eluted with chloroform, whereby 9.64 g of 1α,3β-bis(triethylsilyloxy)-5-androsten-17-one was obtained as a pale yellow crystal. Part of the compound was recrystallized from methanol to give colorless needles having a melting point of 99°-100° C.
後処理
- distillationthe solvent was distilled off under vacuum
- extractionThe residue was subjected to extraction with benzene
- washThe benzene layer was successively washed with an aqueous solution of 0.5N HCl, water, saturated sodium hydrogencarbonate
- dry with materiala saturated aqueous solution of sodium chloride, and dried over magnesium sulfate
- customThe residue obtained
- distillationby distilling off the solvent under vacuum
- washeluted with chloroform
出典と根拠
- ORDレコード
- ord-9ea832c1589043b0a35108158ab39074
- 出典データセット
- uspto-grants-1990_01
- 特許番号
- US04891364
関連ノート
読み込み中…