Реакция #1256709

ord-279712891ed94928b604bb9f9a98351e

Уравнение реакции

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

Растворители

Условия реакции

Температура
60°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураAfter cooling to room temperature
  2. 2
    Концентрированиеthe mixture was concentrated in vacuo

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07824582B2uspto-grants-2010_11