Dimethyl Sulfoxide → tert-Butyl 3-(3-oxopropyl)piperidine-1-carboxylate
反応式
C(Cl)(=O)C(Cl)=O.CS(C)=O.[OH:11][CH2:12][CH2:13][CH2:14][CH:15]1[CH2:20][CH2:19][CH2:18][N:17]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:16]1.C([O-])(O)=O.[Na+]>C(Cl)Cl>[O:11]=[CH:12][CH2:13][CH2:14][CH:15]1[CH2:20][CH2:19][CH2:18][N:17]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:16]1参加物
反応条件
- 温度
- -60 °C
実験手順
An oven-dried 3-neck 1 L round-bottom flask under nitrogen was charged with DCM (100 mL) and oxalyl chloride (1.98 mL, 22.6 mmol) and cooled to −60° C. DMSO (3.21 mL, 45.2 mmol) was added dropwise, and the reaction mixture was stirred for 5 min. A solution of tert-butyl 3-(3-hydroxypropyl)piperidine-1-carboxylate (5.00 g, 20.6 mmol) in DCM (100 mL) was added via addition funnel, and the reaction mixture was stirred for 20 min. TEA (14.3 mL, 103 mmol) was added, and the reaction mixture was warmed slowly to RT. The reaction mixture was poured into 2.5% NaHCO3 and extracted with methylene chloride. The combined organic layers were washed with 5% KHSO4 then brine, dried with anhydrous MgSO4, filtered and concentrated. The product was purified by silica gel chromatography (80 hexane/20 EtOAc). LRMS (M+H)+=242.3.
後処理
- stirringthe reaction mixture was stirred for 20 min
- temperaturethe reaction mixture was warmed slowly to RT
- extractionextracted with methylene chloride
- washThe combined organic layers were washed with 5% KHSO4
- dry with materialbrine, dried with anhydrous MgSO4
- filtrationfiltered
- concentrationconcentrated
- customThe product was purified by silica gel chromatography (80 hexane/20 EtOAc)
出典と根拠
- ORDレコード
- ord-2b67265d443749d09c385701b10ffb6d
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08591878B2
反応ノート
読み込み中…