反应 #2286331

ord-80655e5b7e5c4994bfd49e5b8ffd50bf

反应方程式

OCCc1cc(Cl)c(O)c(Cl)c1
2,6-dichloro-4-(2-hydroxy-ethyl)-phenol
OCCc1cc(Cl)c(O)c(Cl)c1
2,6-Dichloro-4-(2-hydroxy-ethyl)-phenol
CCN(CC)CC
triethylamine
CC(C)(C)[Si](Cl)(c1ccccc1)c1ccccc1
tert-butyl diphenylsilylchloride
CC(C)(C)[Si](OCCc1cc(Cl)c(O)c(Cl)c1)(c1ccccc1)c1ccccc1
4-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,6-dichloro-phenol
收率 60.4%
CC(C)(C)[Si](OCCc1cc(Cl)c(O)c(Cl)c1)(c1ccccc1)c1ccccc1
4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-2,6-dichloro-phenol
收率 60.4%

反应条件

温度
25°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤The organics were washed with a 1N aqueous hydrochloric acid solution, water
  2. 2
    干燥a saturated aqueous sodium chloride solution, dried with magnesium sulfate
  3. 3
    过滤filtered
  4. 4
    浓缩concentrated under vacuum

实验过程

A solution of 2,6-dichloro-4-(2-hydroxy-ethyl)-phenol (16) (2.0 g, 9.66 mmol) in methylene chloride (20 mL) at 25° C. was treated with triethylamine (1.35 mL, 9.66 mmol) and tert-butyl diphenylsilylchloride (2.48 mL, 9.66 mmol). The reaction was stirred at 25° C. for 18 h. At this time, the reaction was diluted with methylene chloride. The organics were washed with a 1N aqueous hydrochloric acid solution, water, and a saturated aqueous sodium chloride solution, dried with magnesium sulfate, filtered and concentrated under vacuum. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 95:5 petroleum ether/ethyl acetate) afforded 4-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,6-dichloro-phenol (70) (2.60 g, 60%) as a pale yellow oil; HRMS m/e calcd for C24H26Cl2O2Si (M+Na)+ 467.0971, found 467.0977. Exact Mass=444.1079; Molecular Weight=445.47.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE046024E1uspto-grants-2016_06