反应 #64356

ord-045e968bcdcc4bc08bd08d84a4d9ffb7

反应方程式

CNC(=O)C1=CC(C)(C)Oc2ccc([N+](=O)[O-])cc21
N-methyl-6-nitro-2,2-dimethyl-2H-1-benzopyran-4-carboxamide
CCI
ethyl iodide
[H-]
hydride
C1CCOC1
tetrahydrofuran
ClCCl
Dichloromethane
CCN(C)C(=O)C1=CC(C)(C)Oc2ccc([N+](=O)[O-])cc21
N-ethyl-N-methyl-6-nitro-2,2-dimethyl-2H-1-benzopyran-4-carboxamide

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度was heated
  2. 2
    温度at reflux for 30 minutes
  3. 3
    其他any insoluble matter was removed by filtration
  4. 4
    其他The filtrate was recrystallized from a mixture of diethyl ether and n-hexane

实验过程

A mixture of 0.53 g of N-methyl-6-nitro-2,2-dimethyl-2H-1-benzopyran-4-carboxamide, 1.60 g of ethyl iodide, 0.09 g of sodlum hydride, and 10 ml of tetrahydrofuran was heated at reflux for 30 minutes. Dichloromethane was added to the reaction mixture, and any insoluble matter was removed by filtration. The filtrate was recrystallized from a mixture of diethyl ether and n-hexane to obtain 0.45 g of N-ethyl-N-methyl-6-nitro-2,2-dimethyl-2H-1-benzopyran-4-carboxamide represented by formula shown below.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05412117uspto-grants-1995_05