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Water → HCID 59633980、化合物

HRID 1615085
ノート
印刷プレビュー

反応式

HRID 1615085 の反応式
[CH2:1]([C:5]1[CH:10]=[CH:9][N:8]=[C:7]([C:11]#[N:12])[CH:6]=1)[CH2:2][CH:3]=[CH2:4].[OH2:13].C[N+]1([O-])CC[O:18]CC1.[O-]S([O-])(=S)=O.[Na+].[Na+]>CC(C)=O.[Os](=O)(=O)(=O)=O>[OH:13][CH:3]([CH2:4][OH:18])[CH2:2][CH2:1][C:5]1[CH:10]=[CH:9][N:8]=[C:7]([C:11]#[N:12])[CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 24477Sodium ThiosulfateHCID 82029Methyl morpholine oxideHCID 59634012HCID 59634012、化合物2 回

生成物 1

HCID 59633980HCID 59633980、化合物収率 72%

試薬・触媒・溶媒 2

HCID 30318Osmium Tetroxide触媒
HCID 180
Acetone
溶媒

実験手順

To a mixed solution of 4-but-3-enyl-pyridine-2-carbonitrile (0.17 g) prepared in (1) in acetone (4 mL)/water (2 mL) were added 4-methylmorpholine N-oxide (0.37 g) and aqueous 4% osmium tetraoxide (0.67 g). The reaction mixture was stirred at RT for 12 hr. Saturated aqueous Na2S2O3 was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, and then dried over Na2SO4. The solvent was removed under reduced pressure. The residue was purified by silica gel chromatography (Developing solvent: chloroform/methanol=15/1) to give the title compound (0.15 g, 72%).

後処理

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with brine
  3. dry with materialdried over Na2SO4
  4. customThe solvent was removed under reduced pressure
  5. customThe residue was purified by silica gel chromatography (Developing solvent: chloroform/methanol=15/1)

出典と根拠

ORDレコード
ord-9ca800461bb94f289ca040c2eb7b266a
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08765739B2

反応ノート

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