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Methyl morpholine oxide → 1-Propylcyclobutane-1-carbaldehyde

HRID 9232
ノート
印刷プレビュー

反応式

HRID 9232 の反応式
C[N+]1([O-])CCOCC1.[CH2:9]([C:12]1([CH2:16][OH:17])[CH2:15][CH2:14][CH2:13]1)[CH2:10][CH3:11]>ClCCl.[Ru]([O-])(=O)(=O)=O.C([N+](CCC)(CCC)CCC)CC>[CH2:9]([C:12]1([CH:16]=[O:17])[CH2:15][CH2:14][CH2:13]1)[CH2:10][CH3:11]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 82029Methyl morpholine oxideHCID 21985998(1-Propylcyclobutyl)methanol2 回

生成物 1

HCID 143013561-Propylcyclobutane-1-carbaldehyde収率 218.9%

試薬・触媒・溶媒 2

HCID 178419074HCID 178419074、化合物触媒HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

An ice-cold mixture of 4-methylmorpholine N-oxide (NMO) (1.683 g, 14.4 mmol), 1-3 (1.229 g, 9.59 mmol) and 4 Å molecular sieves (5.5 g) in dichloromethane (20 mL) was treated with tetrapropylammonium perruthenate (TPAP) (179 mg, 0.51 mmol). The mixture was stirred at 0° C. for 5 min. and then was allowed to warm to room temperature. After 1 h, the mixture was filtered through a pad of silica gel (dichloromethane) and the dichloromethane was evaporated. The crude product was combined with the crude product from another batch (starting with 4.986 g, 38.9 mmol of 1-3) and the combined product was purified by distillation under reduced pressure followed by flash chromatography on silica gel (15% ether/pentane) to give 1-4 (2.649 g, 43%).

後処理

  1. temperatureto warm to room temperature
  2. waitAfter 1 h
  3. filtrationthe mixture was filtered through a pad of silica gel (dichloromethane)
  4. customthe dichloromethane was evaporated
  5. distillationthe combined product was purified by distillation under reduced pressure

出典と根拠

ORDレコード
ord-421cfd5fe897437b9d9739632c65ce27
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07091231B2

反応ノート

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