Hydrogen Peroxide → 3-Acetoxyestra-1,3,5(10)-trien-17-one-2-carboxylic acid
反応式
[C:1]([O:4][C:5]1[C:22]([CH:23]=[O:24])=[CH:21][C:20]2[C@@H:19]3[C@H:10]([C@H:11]4[C@@:15]([CH2:17][CH2:18]3)([CH3:16])[C:14](=[O:25])[CH2:13][CH2:12]4)[CH2:9][CH2:8][C:7]=2[CH:6]=1)(=[O:3])[CH3:2].OO.[OH:28]P([O-])(O)=O.[Na+].Cl([O-])=O.[Na+]>C(#N)C.O>[C:1]([O:4][C:5]1[C:22]([C:23]([OH:28])=[O:24])=[CH:21][C:20]2[C@@H:19]3[C@H:10]([C@H:11]4[C@@:15]([CH2:17][CH2:18]3)([CH3:16])[C:14](=[O:25])[CH2:13][CH2:12]4)[CH2:9][CH2:8][C:7]=2[CH:6]=1)(=[O:3])[CH3:2]参加物
実験手順
To a suspension of 3-acetoxyestra-1,3,5(10)-trien-17-one-2-carboxaldehyde (61, 1.20 g, 3.5 mmol) in acetonitrile (17 mL) and H2O (2.1 mL) were added 30% hydrogen peroxide (0.53 mL) and sodium phosphate monobasic (1.79 g) at room temperature. Sodium chlorite (0.935 g in a H2O (7.0 mL) solution) was added dropwise to the reaction mixture over a 1 h period, and stirring continued for an additional 2 h at room temperature. The reaction mixture was quenched with sodium sulfite, acidified with 10% HCl, and extracted with EtOAc. The combined organic layers were washed with H2O, saturated aqueous NaCl, and then dried (Na2SO4). The desiccant was filtered and the solvent was evaporated at reduced pressure. The residue was washed with Et2O to afford 1.06 g of 62 (85% yield) mp: 180-181° C.
後処理
- customThe reaction mixture was quenched with sodium sulfite
- extractionextracted with EtOAc
- washThe combined organic layers were washed with H2O, saturated aqueous NaCl
- dry with materialdried (Na2SO4)
- filtrationThe desiccant was filtered
- customthe solvent was evaporated at reduced pressure
- washThe residue was washed with Et2O
出典と根拠
- ORDレコード
- ord-642af89248494250ae66c48382be48c8
- 出典データセット
- uspto-grants-2000_04
- 特許番号
- US06046186
反応ノート
読み込み中…