HRID1066818

反应详情

EQUATION

反应方程式

HRID 1066818 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-45 °C

PROCEDURE

实验过程

A stirred solution of 4-(t-butoxycarbonylamino)-4,4-dimethylbutan-1-ol (1.11 g, 5.11 mmol) in tetrahydrofuran (49 ml) at −45° C. was treated with potassium t-butoxide (1 M in tetrahydrofuran, 5.62 ml, 5.62 mmol). The anion was stirred for 30 minutes at −45° C., then cooled to −78° C. and treated with a tetrahydrofuran solution of 2-fluoro-5-bromobenzyl bromide (1.23 g, 4.60 mmol). The resulting yellow mixture was slowly warmed to 0° C. and stirred for about four hours. The reaction mixture was diluted wtih methylene chloride (100 ml) and washed with 1 M potassium carbonate (20 ml). The organic fraction was dried over sodium sulfate, filtered, and the solvents were removed in vacuo. The residue was further purified by preparative high performance liquid chromatography to yield 1.53 grams (74%) of the title intermediate as a colorless oil.

WORKUP

后处理

  1. temperaturecooled to −78° C.
  2. temperatureThe resulting yellow mixture was slowly warmed to 0° C.
  3. stirringstirred for about four hours
  4. washwashed with 1 M potassium carbonate (20 ml)
  5. dry with materialThe organic fraction was dried over sodium sulfate
  6. filtrationfiltered
  7. customthe solvents were removed in vacuo
  8. customThe residue was further purified by preparative high performance liquid chromatography