反应 #49893

ord-10bd30426ab0424eb72c822219e8e9e9

反应方程式

CI
methyl iodide
COC(Cl)Cl
dichloromethyl methyl ether
[Cl][Sn]([Cl])([Cl])[Cl]
tin tetrachloride
CC(C)(C)c1cccc(C(C)(C)C)c1O
2,6-di-tert-butyl phenol
[Na+].[OH-]
NaOH
COc1c(C(C)(C)C)cc(C=O)cc1C(C)(C)C
3,5-di-tert-butyl-4-methoxybenzaldehyde
收率 47.7%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他After purification 0.67 g 2,6-di-tert-butyl anisol
  2. 2
    其他was obtained

实验过程

A mixture containing 2 g (9.7 mmol) 2,6-di-tert-butyl phenol, 0.4 g NaOH dissolved in 4 ml water, 13.7 g (60.1 mmol) benzyl triethyl ammonium chloride and 12 g (84.5 mmol) methyl iodide was heated at 45° for 18 h. After purification 0.67 g 2,6-di-tert-butyl anisol was obtained. This compound (1.46 g, 6.63 mmol) was formylated by reaction at 0° C. with dichloromethyl methyl ether (1.15 g, 10 mmol) in presence of tin tetrachloride (3.1 g, 11.9 mmol) in 20 ml CH2Cl2. After hydrolysis and extraction into ether, 1.15 g of 3,5-di-tert-butyl-4-methoxybenzaldehyde were obtained (MS: m/e=248: M+; 233=M+ --CH3).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05424303uspto-grants-1995_06