反応式
[C:1](=[O:4])([O-])[O-].[K+].[K+].C1(C)C=CC=CC=1.[CH2:14]=[CH:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]C.S([O-])([O-])=[O:25].[Na+].[Na+]>C(O)(C)(C)C.O.[Fe-3](C#N)(C#N)(C#N)(C#N)(C#N)C#N.[K+].[K+].[K+].[Os](=O)(=O)(=O)=O.C(OCC)(=O)C>[CH2:1]([OH:4])[CH:22]([OH:25])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH3:14]参加物
反応条件
- 温度
- 0 °C
実験手順
To a well-stirred solution of bis-1,4-(9'-O-dihydroquinidine)phthalazine (7.8 mg, 0.01 mmol), potassium ferricyanide (0.99 g, 3 mmol), potassium carbonate (0.42 g, 3 mmol), and osmium tetroxide (0.1 mL of a 0.1M toluene solution, 0.01 mmol) in 15 mL of a tert-butyl alcohol-water (1:1, v/v) at 0° C., 1-decene (0.14 g, 0.19 mL, 1 mmol) was added in one portion. The mixture was stirred for 24 h at 0° C. Solid sodium sulfite (1.5 g) was added and the mixture was stirred for an additional hour, and then warmed up to room temperature. Ethyl acetate (10 mL) was added to the reaction mixture, and aqueous layer was extracted with ethyl acetate (3×5 mL). Combined organic layer was dried over anhydrous magnesium sulfate, and concentrated in vacuo. Crude product was purified by flash chromatography (silica gel, hexanes/EtOAc) to afford decane 1,2-diol as a white solid (0.145 g, 83%). HPLC analysis of the bis-Mosher ester of this crude decane 1,2 diol gave 84% ee.
後処理
- stirringthe mixture was stirred for an additional hour
- temperaturewarmed up to room temperature
- extractionwas extracted with ethyl acetate (3×5 mL)
- dry with materialCombined organic layer was dried over anhydrous magnesium sulfate
- concentrationconcentrated in vacuo
- customCrude product was purified by flash chromatography (silica gel, hexanes/EtOAc)
出典と根拠
- ORDレコード
- ord-5d317fd0c8aa4f019316bfb9a8cfe508
- 出典データセット
- uspto-grants-1993_11
- 特許番号
- US05260461
関連ノート
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