反応式
[CH2:1]([N:8]1[CH2:13][CH2:12][C:11](=O)[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl-].[CH3:16][O:17][NH3+:18]>>[CH2:1]([N:8]1[CH2:13][CH2:12][C:11](=[N:18][O:17][CH3:16])[CH2:10][CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
3
実験手順
The starting material is prepared as follows: The solution of 94.5 g of 1-benzyl-4-piperidone and 46 g of methoxyammonium chloride in 600 ml of ethanol-pyridine (1:1) is refluxed overnight and evaporated. The residue is dissolved in water, the solution made basic with 12.5% aqueous sodium hydroxide and extracted with diethyl ether. The extract is washed with water and saturated aqueous sodium hydroxide, dried and evaporated, to yield the 1-benzyl-4-methoxyiminopiperidine.
後処理
- customThe starting material is prepared
- customevaporated
- dissolutionThe residue is dissolved in water
- extractionextracted with diethyl ether
- washThe extract is washed with water and saturated aqueous sodium hydroxide
- customdried
- customevaporated
出典と根拠
- ORDレコード
- ord-2a1f8645fcbd4743829f06767cb00f3d
- 出典データセット
- uspto-grants-1979_04
- 特許番号
- US04147786
関連ノート
読み込み中…