HRID1358050

反应详情

EQUATION

反应方程式

HRID 1358050 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

A mixture of 1-(4-bromobenzyl)-6-phenylmethoxy-2-(4-fluorophenyl)-1,2,3,4-tetrahydroisoquinoline (1.0 g, 1.99 mmol), dibenzylideneacetone palladium (36 mg, 0.04 mmol), BINAP (74 mg, 0.12 mmol), sodium tert-butoxide (0.29 g, 3.0 mmol) and N-acetylpiperazine (0.38 g, 3.0 mmol) in 2 ml of toluene were added to a sealed tube under an argon atmosphere and heated at 80° C. for 16 h. The sealed tube was cooled to room temperature and the contents of the tube transferred to a separatory funnel. Ethyl acetate and water were added and the organic layer was separated. The combined organic layers were dried over MgSO4, concentrated, and purified by column chromatography (SiO2, chloroform/methanol, 99:1) to provide the title compound (0.45 g, 41% yield): ES-MS (m/z) 550 [M+H]+.

WORKUP

后处理

  1. additionwere added to a sealed tube under an argon atmosphere
  2. temperatureThe sealed tube was cooled to room temperature
  3. customthe contents of the tube transferred to a separatory funnel
  4. customthe organic layer was separated
  5. dry with materialThe combined organic layers were dried over MgSO4
  6. concentrationconcentrated
  7. custompurified by column chromatography (SiO2, chloroform/methanol, 99:1)