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硼11三氟化硼气体 → 2-Ethoxycarbonyl-5-aminocycloheptanone

HRID 726331
笔记
打印预览

反应方程式

HRID 726331 反应方程式
[NH2:1][CH:2]1[CH2:7][CH2:6][C:5](=[O:8])[CH2:4][CH2:3]1.B(F)(F)F.[N+](=[CH:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[N-]>C(OCC)C>[CH2:19]([O:18][C:16]([CH:15]1[CH2:6][CH2:7][CH:2]([NH2:1])[CH2:3][CH2:4][C:5]1=[O:8])=[O:17])[CH3:20]
参与物实验过程来源与证据反应笔记

参与物

5

反应物 3

HCID 6356硼11三氟化硼气体HCID 12192重氮乙酸乙酯HCID 99123064-氨基环己酮

产物 1

HCID 226116412-Ethoxycarbonyl-5-aminocycloheptanone

试剂、催化剂与溶剂 1

HCID 3283乙醚溶剂

实验过程

The appropriate 4-aminocyclohexanone in an appropriate solvent, for example diethyl ether, is treated with an appropriate Lewis acid such as boron trifluoride for about 20 minutes to about an hour at room temperature. To this solution is then added ethyl diazoacetate and the resulting mixture is stirred for about 1 hour to about 24 hours at room temperature. The resulting 2-ethoxycarbonyl-5-aminocycloheptanone is isolated by diluting the reaction mixture with aqueous sodium carbonate and extracting with a water immiscible solvent such as diethyl ether. The reaction product is then directly dissolved in dimethylsulfoxide which contains sodium chloride and water. The reaction mixture is heated to about 170° for from about 1 to about 24 hours to effect the decarboxylation. The desired 4-aminocycloheptanone is recovered by diluting the reaction mixture with water and extracting with an appropriate solvent such as diethyl ether. The reaction product may be purified by column chromatography, if desired, prior to further reaction.

来源与证据

ORD记录
ord-3061a7decd494353b04fe8e14508c179
来源数据集
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
专利号
US05708187

反应笔记

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本页导航参与物实验过程来源与证据反应笔记