Phosgene → Ethyl 1-(chlorocarbonyl)piperidine-2-carboxylate
反応式
[CH2:1]([O:3][C:4]([CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][NH:7]1)=[O:5])[CH3:2].C(N(CC)CC)C.[C:19](Cl)([Cl:21])=[O:20]>C1C=CC=CC=1>[Cl:21][C:19]([N:7]1[CH2:8][CH2:9][CH2:10][CH2:11][CH:6]1[C:4]([O:3][CH2:1][CH3:2])=[O:5])=[O:20]参加物
5
実験手順
A mixture of 2-ethoxycarbonylhexahydropyridine (5 g, 32 mmol) and triethylamine (3.2 g, 32 mmol) in 15 ml of benzene is added dropwise to phosgene, with ice-bath cooling. After the addition is complete, the mixture is allowed to warm to RT and is stirred for 2 hours. The reaction is diluted with benzene to about 150 ml, washed with water (3X), dried over sodium sulfate and stripped to give N-chlorocarbonyl-2-ethoxycarbonylhexahydropyridine.
後処理
- temperaturecooling
- additionAfter the addition
- washwashed with water (3X)
- dry with materialdried over sodium sulfate
出典と根拠
- ORDレコード
- ord-4a7e811dbf7243078666d6cd19cd9139
- 出典データセット
- uspto-grants-1983_09
- 特許番号
- US04406689
反応ノート
読み込み中…