تفاعل #1256709

ord-279712891ed94928b604bb9f9a98351e

معادلة التفاعل

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

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAfter cooling to room temperature
  2. 2
    تركيزthe mixture was concentrated in vacuo

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07824582B2uspto-grants-2010_11