Dimethyl Sulfoxide → tert-Butyl 3-(3-oxopropyl)piperidine-1-carboxylate

HRID 2045693ノート

反応式

HRID 2045693 の反応式
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

6

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

  1. stirringthe reaction mixture was stirred for 20 min
  2. temperaturethe reaction mixture was warmed slowly to RT
  3. extractionextracted with methylene chloride
  4. washThe combined organic layers were washed with 5% KHSO4
  5. dry with materialbrine, dried with anhydrous MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. 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

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