Sodium Sulfite → (1S,4S,6R)-4-benzhydryl-3,7-dioxa-bicyclo[4.1.0]-heptane
反応式
[CH:1]([C@@H:14]1[CH2:19][CH:18]=[CH:17][CH2:16][O:15]1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1C=C(Cl)C=C(C(OO)=[O:28])C=1.[O-]S([O-])=O.[Na+].[Na+]>C(Cl)Cl>[CH:1]([C@@H:14]1[CH2:19][C@@H:18]2[C@@H:17]([O:28]2)[CH2:16][O:15]1)([C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
実験手順
To a solution of (2S)-2-benzhydryl-3,6-dihydro-2H-pyran 27a (0.15 g, 0.6 mmol) in CH2Cl2 (20 ml) was added mCPBA (0.3 g, 70%, 1.2 mmol) in a portionwise manner at 0° C. The mixture was brought to room temperature and the reaction mixture was stirred for 20 h under N2. Na2SO3 (20 ml 1.0 M solution) was added to the reaction mixture at 0° C. to quench the reaction. The aqueous phase was extracted with CH2Cl2 (20 ml×2). The combined organic phase was washed in turn with saturated NaHCO3 and brine, then dried over anhydrous Na2SO4. Evaporation of the solvent gave light brown solid residue. The crude products were purified by flash chromatography on silica gel (hexane/ethyl ether=9:1) to give 0.08 g (1S,4S,6R)-4-benzhydryl-3,7-dioxa-bicyclo[4.1.0]-heptane 28a (50.3%, [α]D=(−)60, c=1, MeOH) and 0.065 g 28b (1R,4S,6S)-4-benzhydryl-3,7-dioxa-bicyclo[4.1.0]-heptane (41%, [α]D=(−) 76, c=1, MeOH).
後処理
- customwas brought to room temperature
- customto quench
- customthe reaction
- extractionThe aqueous phase was extracted with CH2Cl2 (20 ml×2)
- washThe combined organic phase was washed in turn with saturated NaHCO3 and brine
- dry with materialdried over anhydrous Na2SO4
- customEvaporation of the solvent
- customgave light brown solid residue
- customThe crude products were purified by flash chromatography on silica gel (hexane/ethyl ether=9:1)
出典と根拠
- ORDレコード
- ord-632f632183384da3aee6972c4a64dcfa
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08841464B2
反応ノート
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