反应 #75449

ord-27e45ce573f248c2970b44111ba6282b

反应方程式

Cl
HCl
Cl
HCl
CC(C)=CCCn1ccnc1[N+](=O)[O-]
4-Methyl-1-(2-nitro-1H-imidazol-1-yl)-3-pentene
CC(C)CCON=O
isoamyl nitrite
Cl
HCl
CC(C)(Cl)C(CCn1ccnc1[N+](=O)[O-])N=O
title product
收率 81.0%
CC(C)(Cl)C(CCn1ccnc1[N+](=O)[O-])N=O
4-Chloro-4-methyl-1-(2-nitro-1H-imidazol-1-yl)-3-nitrosopentane
收率 81.0%

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The product was filtered
  2. 2
    洗涤washed with ethanol-ether (1:2)
  3. 3
    其他dried in vacuum

实验过程

4-Methyl-1-(2-nitro-1H-imidazol-1-yl)-3-pentene (8 g, 41 mmol) was dissolved in isoamyl nitrite (50 mL) at room temperature. The solution was cooled to 0° C. in an ice-salt bath and concentrated HCl (12 mL) was added dropwise. The reaction temperature was maintained between 3-5° C. during the HCl addition; the reaction was stirred in an ice-salt bath for 45 minutes after the addition of HCl. The product was filtered, washed with ethanol-ether (1:2) and dried in vacuum to give 8.6 g (81%) of the title product as a white solid; mp: 96-97° C. MS: (M+H)+=261, M+=260. 1H NMR (DMSO-d6) δ1.70 (s, 6H, gem-di-CH3), 2.94 (t, 2H, CH2C═NOH), 4.65 [t, 2H, CH2-(2-nitroimidazole)], 7.16 and 7.52 (s, 2H, 2-nitroimidazolyl-H), 11.43 (s, 1H, CH2C═NOH).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06699458B2uspto-grants-2004_03