反応式
[P:1]([O-:12])([O:7][C:8]([CH3:11])([CH3:10])[CH3:9])[O:2][C:3]([CH3:6])([CH3:5])[CH3:4].C[Si]([N-][Si](C)(C)C)(C)C.[Li+].[Br:23][CH2:24][C:25]1[CH:32]=[CH:31][C:28]([CH:29]=[O:30])=[C:27]([Br:33])[CH:26]=1.C([O-])(=O)C.[NH4+]>C1COCC1>[Br:33][C:27]1[CH:26]=[C:25]([CH2:24][Br:23])[CH:32]=[CH:31][C:28]=1[CH:29]([P:1](=[O:12])([O:7][C:8]([CH3:11])([CH3:10])[CH3:9])[O:2][C:3]([CH3:5])([CH3:6])[CH3:4])[OH:30]参加物
反応条件
- 温度
- -78 °C
実験手順
Di-tert-butyl phosphite (14.8 g, 76.3 mmol, 1.05 eq) was dissolved in 200 ml THF at −78° C. under nitrogen and 72 ml (1.05 eq) of 1.06M Lithium bis(trimethylsilyl)amide in THF was added over 30 min. The mixture was left stirring at −78° C. under nitrogen for 30 min and then added to a solution of the compound of Step 3 (20.2 g, 72.7 mmol, 1 eq) in 200 ml THF at −78° C. The solution was warmed to 0° C. and then poured into 400 ml of half saturated aqueous ammonium acetate. The layers were separated and the aqueous layer was washed with 400 ml isopropyl acetate. The organic layers were combined, dried with sodium sulfate and the solvent removed. The crude solid was then triturated with 15% EtOAc/hexane for 2 hours and 30.4 g (89%) of the title compound was obtained.
後処理
- waitThe mixture was left
- temperatureThe solution was warmed to 0° C.
- customThe layers were separated
- washthe aqueous layer was washed with 400 ml isopropyl acetate
- dry with materialdried with sodium sulfate
- customthe solvent removed
- customThe crude solid was then triturated with 15% EtOAc/hexane for 2 hours
出典と根拠
- ORDレコード
- ord-9d72a0551e864d5489519bd0482b2197
- 出典データセット
- uspto-grants-2004_08
- 特許番号
- US06777433B2
関連ノート
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