反应 #1256709

ord-279712891ed94928b604bb9f9a98351e

反应方程式

Cc1cncc(C)c1-c1c(C)cc(O)cc1C
6
Cc1cncc(C)c1-c1c(C)cc(O)cc1C
4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenol
CI
iodomethane
Cc1cc(O)cc(C)c1-c1c(C)c[n+](C)cc1C.[I-]
methyl pyridinium iodide salt
Cc1cc(O)cc(C)c1-c1c(C)c[n+](C)cc1C.[I-]
4-(4-hydroxy-2,6-dimethyl-phenyl)-1,3,5-trimethyl-pyridinium iodide

溶剂

反应条件

温度
60°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度After cooling to room temperature
  2. 2
    浓缩the mixture was concentrated in vacuo

实验过程

To a stirring solution of 6 (0.113 g, 0.500 mmol) in anhydrous methanol (10 mL) was added dropwise iodomethane (0.5 mL, 0.660 g, 2.75 mmol) at room temperature under N2. The reaction mixture was then stirred at 60° C. under N2 overnight. After cooling to room temperature, the mixture was concentrated in vacuo to give the corresponding methyl pyridinium iodide salt as an analytically pure yellow solid (0.184 g, 99.4%). mp 257-258° C.; 1H NMR (500 MHz, DMSO-d6): δ 9.562 (s, 1H), 8.898 (s, 2H), 6.645 (s, 2H), 4.295(s, 3H), 2.015 (s, 6H), 1.760 (s, 6H); 13C NMR (125 MHz, DMSO-d6): δ 157.588, 157.448, 143.158, 136.942, 134.675, 124.179, 114.988, 47.297, 19.162, 16.527; MS (ESI): m/z 242.4 [(M−I)+, 100]; Anal. Calcd. For C16H20INO·H2O: C, 49.62; H, 5.73; N, 3.62; I, 32.77. Found: C, 50.08; H, 5.52; N, 3.65; I, 33.49.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07824582B2uspto-grants-2010_11