Triacetoxyperiodinane → 2-(4-Fluoro-phenyl)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester
反応式
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH2:10][C:9]1([C:15]1[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=1)[CH2:13][OH:14])=[O:7])([CH3:4])([CH3:3])[CH3:2].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>C(Cl)Cl>[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH2:10][C:9]1([C:15]1[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=1)[CH:13]=[O:14])=[O:7])([CH3:4])([CH3:2])[CH3:3]参加物
実験手順
To 2-(4-fluoro-phenyl)-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (3.9 g) in a round bottom flask was added Dess-Martin periodinane solution (47 mL of a 15% solution in DCM, CAS [87413-09-0]) and the reaction mixture was stirred for 5 hours at RT. The reaction mixture was then quenched with saturated aqueous sodium thiosulfate solution (25 mL) and stirred a further 20 minutes. The phases were separated and the aqueous was extracted with further DCM (25 mL). The combined organic phases were washed with saturated sodium bicarbonate solution and dried over sodium sulfate. Filtration of the drying agent and evaporation of the volatiles in vacuo afforded the desired 2-(4-fluoro-phenyl)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (4.13 g, MS (ES+): 294.1 (MH+)) as a brown solid which was taken into the next step without further purification.
後処理
- customThe reaction mixture was then quenched with saturated aqueous sodium thiosulfate solution (25 mL)
- stirringstirred a further 20 minutes
- customThe phases were separated
- extractionthe aqueous was extracted with further DCM (25 mL)
- washThe combined organic phases were washed with saturated sodium bicarbonate solution
- dry with materialdried over sodium sulfate
- filtrationFiltration of the drying agent and evaporation of the volatiles in vacuo
出典と根拠
- ORDレコード
- ord-0743f584853140efbd7affb7db0cec47
- 出典データセット
- uspto-grants-2012_02
- 特許番号
- US08124636B2
反応ノート
読み込み中…