反应 #69653

ord-a8c909eaca664dc2a9a6be3fc4c15e79

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度at reflux for 3 hours
  2. 2
    温度Upon cooling the solvent
  3. 3
    其他was removed in vacuo
  4. 4
    其他the mixture partitioned between dichloromethane and water
  5. 5
    其他The organics were separated
  6. 6
    其他the solvent removed in vacuo

实验过程

Ethyl 4-hydroxybenzoate (1.66 g, 10.0 mmol) and anhydrous potassium carbonate (2.07 g, 15.0 mmol) in acetonitrile (30 ml) was treated with 3-methyl-2-butenyl chloride (1.35 ml, 12.0 mmol) and the mixture was stirred and held at reflux for 3 hours. Upon cooling the solvent was removed in vacuo and the mixture partitioned between dichloromethane and water. The organics were separated and the solvent removed in vacuo to afford ethyl 4-(3-methyl-but-2-enyloxy)-benzoate (2.23 g, 95%) as a pale yellow liquid which was used without further purification. 1H NMR (DMSO-d6) 7.89 (2H, d), 7.04 (2H, d), 5.44 (1H, t), 4.62 (2H, d), 4.28 (2H, q), 1.77 (3H, s), 1.73 (3H, s), 1.31 (3H, t). MS: [M+H]+ 235.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08530469B2uspto-grants-2013_09