HRID495015

反应详情

EQUATION

反应方程式

HRID 495015 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-20 °C

PROCEDURE

实验过程

A solution of 1-bromo-4-chloro-2-fluorobenzene (20.4 g, 0.100 mol) in tetrahydrofuran (THF; 50 mL) was slowly added to lithium diisopropylamide (LDA; 0.125 mol) in THF (600 mL) at −50° C. After addition, the solution was warmed to −20° C. and then cooled to −50° C. A solution of trimethyl borate (13.5 g, 0.130 mol) in THF (20 mL) was added slowly and the temperature was warmed to −20° C. The mixture was then cooled to −70° C. and a solution of peracetic acid (32% in acetic acid, 0.150 mol) was slowly added and the mixture was warmed to ambient temperature. Water (250 mL) was added and the solution was extracted with ethyl acetate (2×200 mL). The combined organic phases were dried and concentrated. The black oil was purified by column chromatography (20% ethyl acetate in hexanes) to give 3-bromo-6-chloro-2-fluorophenol (14.1 g, 0.063 mol) 1H NMR (CDCl3): δ 7.05 (m, 2H), 5.5 (br s, 1H).

WORKUP

后处理

  1. additionAfter addition
  2. temperaturecooled to −50° C
  3. temperaturethe temperature was warmed to −20° C
  4. temperatureThe mixture was then cooled to −70° C.
  5. temperaturethe mixture was warmed to ambient temperature
  6. extractionthe solution was extracted with ethyl acetate (2×200 mL)
  7. customThe combined organic phases were dried
  8. concentrationconcentrated
  9. customThe black oil was purified by column chromatography (20% ethyl acetate in hexanes)