反応 #1256707

ord-9abd44695a1e4f5e9c10b0134b0cf9e7

反応方程式

COc1cc(C)c(-c2c(C)cncc2C)c(C)c1
4
COc1cc(C)c(-c2c(C)cncc2C)c(C)c1
4-(4-methoxy-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridine
CI
iodomethane
COc1cc(C)c(-c2c(C)c[n+](C)cc2C)c(C)c1.[I-]
methyl pyridinium iodide salt
COc1cc(C)c(-c2c(C)c[n+](C)cc2C)c(C)c1.[I-]
4-(4-methoxy-2,6-dimethyl-phenyl)-1,3,5-trimethyl-pyridinium iodide

溶媒

反応条件

温度
60°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

To a solution of 4 (0.241 g, 1.00 mmol) in dry CH2Cl2 (5 mL) was added dropwise iodomethane (0.32 mL, 0.729 g, 5.10 mmol) at room temperature under N2. The reaction mixture was then refluxed at 60° C. under N2 for 1 h. 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 (0.382 g, 99.8%). mp 220-221° C.; 1H NMR (400 MHz, CD2Cl2): δ 9.079 (s, 2H), 6.751 (s, 2H), 4.579 (s, 3H), 3.881 (s, 3H), 2.135 (s, 6H), 1.854 (s, 6H); 13C NMR (100 MHz, CD2Cl2): δ 160.512, 159.866, 143.124, 138.802, 135.527, 125.927, 114.217, 55.692, 48.686, 20.188, 17.331; Anal. Calcd. For C17H22INO: C, 53.27; H, 5.79; N, 3.65. Found: C, 53.15; H, 5.79; N, 3.57.

出典

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