HRID52568

反应详情

EQUATION

反应方程式

HRID 52568 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a refluxed stirred mixture of 1.34 kg (55.8 moles) of magnesium in 6 L of t-butylmethyl ether (MTBE) and 4 g (0.016 moles) of iodine, a solution of 10 kg (55.9 moles) cyclohexylmethyl bromide in 22 L (MTBE) was added slowly. After approximately 10% to 25% of the solution was added, heating was discontinued and the remainder of the solution was added at a rate to maintain refluxing temperature. After the addition, the reaction was refluxed for an additional 24 hrs, then cooled to 0° to 5° C. and 3.903 kg (37.1 moles) of 2-cyanopyridine in 22 L MTBE was added at 0°-10° C. After the addition, the greenish thick suspension was stirred without cooling for 18-24 hrs. The Grignard reaction mixture was transferred with stirring to 40 L of methanol at 10° to 15° C. To the clear solution was added 1.4 kg (36.8 moles) of sodium borohydride. The mixture was stirred at room temperature 18 hrs., then quenched by the addition of 16 L of water and 36 L of 4N hydrochloric acid. The organic solvents were removed under vacuum and the remaining aqueous solution was washed twice with 6 L of methylene chloride. The aqueous phase was basified with 15 L of ammonium hydroxide solution and extracted three times with 10 L of methylene chloride. The methylene chloride was dried over 6.5 kg of sodium sulfate and concentrated to yield 5.645 kg (75%) of 1-(R,S)-(2-pyridyl)-2-cyclohexylethylamine.

WORKUP

后处理

  1. temperatureheating
  2. additionthe remainder of the solution was added at a rate
  3. temperatureto maintain
  4. temperaturerefluxing temperature
  5. additionAfter the addition
  6. temperaturethe reaction was refluxed for an additional 24 hrs
  7. temperaturecooled to 0° to 5° C.
  8. additionAfter the addition
  9. stirringthe greenish thick suspension was stirred
  10. temperaturewithout cooling for 18-24 hrs
  11. customThe Grignard reaction mixture
  12. stirringThe mixture was stirred at room temperature 18 hrs
  13. custom, then quenched by the addition of 16 L of water and 36 L of 4N hydrochloric acid
  14. customThe organic solvents were removed under vacuum
  15. washthe remaining aqueous solution was washed twice with 6 L of methylene chloride
  16. extractionextracted three times with 10 L of methylene chloride
  17. dry with materialThe methylene chloride was dried over 6.5 kg of sodium sulfate
  18. concentrationconcentrated