HRID1448537

反应详情

EQUATION

反应方程式

HRID 1448537 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution consisting of 42.71 gm. (0.139 mole) of the dimethyl ester of 4-(p-fluorophenyl)-4-cyanopimelic acid (prepared in Part A, above) and 900 ml. tetrahydrofuran is added 31.3 gm. (0.28 mole) potassium tert-butoxide. This reaction mixture is heated at the reflux temperature for four and one half (41/2) hours. It is allowed to cool. It is then chilled in ice and 225 ml. of 2.5 N aqueous acetic acid is added. The organic layer that forms is recovered and diluted with 750 ml. benzene. The benzene:tetrahydrofuran solution is washed successively with sodium bicarbonate, with water, and finally with brine. The solvents are then removed by evaporation under reduced pressure to give 35.6 gm. (93% yield) of 2-carbomethoxy-4-cyano-4-(p-fluorophenyl)cyclohexanone as a gum.

WORKUP

后处理

  1. temperatureto cool
  2. temperatureIt is then chilled in ice
  3. customThe organic layer that forms is recovered
  4. additiondiluted with 750 ml
  5. washThe benzene:tetrahydrofuran solution is washed successively with sodium bicarbonate, with water
  6. customThe solvents are then removed by evaporation under reduced pressure
  7. customto give 35.6 gm