HRID619975

反应详情

EQUATION

反应方程式

HRID 619975 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

A mixture of N-(t-butoxycarbonyl)-2-fluoroaniline (5.0 g, 24 mmoles) in anhydrous tetrahydrofuran (50 ml) was cooled to -78° C. under a nitrogen atmosphere. To this solution was added t-butyl lithium (2.0M, 57.6 mmoles, 28.8 ml) at such a rate that the temperature did not exceed -65° C. When the addition was complete, the mixture was stirred at -78° C. for an additional 15 minutes and at -20° C. for 2.5 hours. To this reaction mixture was added dimethyl disulfide (2.82 g, 30 mmoles) in 10 ml of anhydrous tetrahydrofuran while maintaining the temperature at -20° C. for an additional hour. The mixture was allowed to warm to ambient temperature and then 25 ml of 1N sodium hydroxide was added. The mixture obtained was extracted with diethyl ether (2×100 ml). The organic phase was separated and dried over magnesium sulfate and then the solvent was removed by evaporation under reduced pressure to obtain a tan solid. This was hydrolized in dilute hydrochloric acid (6N, 200 ml) by heating to reflux for three hours. The resulting solution was extracted with diethyl ether and the aqueous layer was neutralized with sodium hydroxide (6N, 200 ml), and extracted with methylene chloride, dried over magnesium sulfate and the solvent removed by evaporation under reduced pressure to obtain an amber oil. This was distilled to give 3.2 g (85% of theory) of the title compound, having a b.p. of 62°-65° C. at 0.2 mm Hg.

WORKUP

后处理

  1. customdid not exceed -65° C
  2. additionWhen the addition
  3. temperaturewhile maintaining the temperature at -20° C. for an additional hour
  4. temperatureto warm to ambient temperature
  5. customThe mixture obtained
  6. extractionwas extracted with diethyl ether (2×100 ml)
  7. customThe organic phase was separated
  8. dry with materialdried over magnesium sulfate
  9. customthe solvent was removed by evaporation under reduced pressure
  10. customto obtain a tan solid
  11. temperatureby heating
  12. temperatureto reflux for three hours
  13. extractionThe resulting solution was extracted with diethyl ether
  14. extractionextracted with methylene chloride
  15. dry with materialdried over magnesium sulfate
  16. customthe solvent removed by evaporation under reduced pressure
  17. customto obtain an amber oil
  18. distillationThis was distilled