반응 #64356

ord-045e968bcdcc4bc08bd08d84a4d9ffb7

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도at reflux for 30 minutes
  3. 3
    기타any insoluble matter was removed by filtration
  4. 4
    기타The filtrate was recrystallized from a mixture of diethyl ether and n-hexane

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05412117uspto-grants-1995_05