Ammonium Chloride → (2S,4R)-Tert-butyl 2-(hydroxymethyl)-4-(methylsulfonyloxy)pyrrolidine-1-carboxylate
反応式
[BH4-].[Li+].[C:3]([O:7][C:8]([N:10]1[CH2:14][C@H:13]([O:15][S:16]([CH3:19])(=[O:18])=[O:17])[CH2:12][C@H:11]1[C:20](OC)=[O:21])=[O:9])([CH3:6])([CH3:5])[CH3:4].[Cl-].[NH4+]>O1CCCC1>[C:3]([O:7][C:8]([N:10]1[CH2:14][C@H:13]([O:15][S:16]([CH3:19])(=[O:17])=[O:18])[CH2:12][C@H:11]1[CH2:20][OH:21])=[O:9])([CH3:6])([CH3:5])[CH3:4]参加物
実験手順
Lithium borohydride (3.6 g, 163.0 mM) was added to a solution of methyl (2S,4R)-N-tert-butoxycarbonyl-4-methanesulfonyloxypyrrolidine-2-carboxylate (26.5 g, 81.5 mM) in anhydrous tetrahydrofuran (300 ml) with ice-cooling in a nitrogen gas stream and the mixture was stirred at room temperature for 3 hours. The reaction mixture was ice-cooled again, the reaction was ceased by adding dropwise a saturated aqueous solution of ammonium chloride carefully and the solvent was removed. The residue was poured into water, the insoluble matters were dissolved using 1N hydrochloric acid, the mixture was extracted with ethyl acetate and the organic layer was washed with 1N hydrochloric acid, water, a saturated aqueous solution of sodium bicarbonate, water and brine in this order and dried over anhydrous magnesium sulfate. The solvent was removed to give the title compound almost quantitatively (24 g).
後処理
- temperaturecooling in a nitrogen gas stream
- temperaturecooled again
- customthe solvent was removed
- additionThe residue was poured into water
- dissolutionthe insoluble matters were dissolved
- extractionthe mixture was extracted with ethyl acetate
- washthe organic layer was washed with 1N hydrochloric acid, water
- dry with materiala saturated aqueous solution of sodium bicarbonate, water and brine in this order and dried over anhydrous magnesium sulfate
- customThe solvent was removed
出典と根拠
- ORDレコード
- ord-478ccce7d7004b82a690401964688549
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06372914B1
反応ノート
読み込み中…