HRID1299

反应详情

EQUATION

反应方程式

HRID 1299 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
65 °C

PROCEDURE

实验过程

73 g (containing 0.25 mole (R)-tert-leucinol) of the filtrate cited in example 6 was taken up with 27 ml water and 200 ml toluene. 25 ml (0.26 mole) chloroformic acid ethyl ester were then added dropwise at 20°-25° C., during which the pH was maintained at 7-8.5 by the addition of 10 M sodium hydroxide solution. The mixture was then heated to 60°-65° C. at pH 8.0 and the aqueous phase separated. The toluene phase was dehydrated on a water separator under a slight vacuum and slowly heated after the addition of 0.4 g finely granulated sodium hydroxide at 70° C. A total of 40 ml distillate which contained the ethanol produced during the reaction was separated from 70°-100° C . After cooling of the batch to 65° C. a solution of 0.6 ml glacial acetic acid in 10 ml water was added, the mixture briefly agitated, the aqueous phase separated and the toluene phase compounded again with 15 ml warm water which was separated again after a brief agitation at 65° C. After distilling the organic phase on a water separator the phase was concentrated to 120 ml, filtered hot and slowly cooled off under agitation, during which the product separated in colorless crystals. These crystals were filtered off after 30 min agitation at 5° C., washed with cold toluene and dried in a vacuum at 50° C. 28.6 g (R)-4-tert-butyl-2-oxazolidinone (80% yield) was obtained. A 1H-NMR spectrum corroborated the structure of the product.

WORKUP

后处理

  1. temperatureThe mixture was then heated to 60°-65° C. at pH 8.0
  2. customthe aqueous phase separated
  3. temperatureslowly heated
  4. additionafter the addition of 0.4 g finely granulated sodium hydroxide at 70° C
  5. customproduced during the reaction
  6. customwas separated from 70°-100° C
  7. additionwas added
  8. customthe aqueous phase separated
  9. temperaturewarm water which
  10. customwas separated again after a brief agitation at 65° C
  11. distillationAfter distilling the organic phase on a water separator the phase
  12. concentrationwas concentrated to 120 ml
  13. filtrationfiltered hot
  14. temperatureslowly cooled off under agitation, during which the product
  15. customseparated in colorless crystals
  16. filtrationThese crystals were filtered off after 30 min agitation at 5° C.
  17. washwashed with cold toluene
  18. customdried in a vacuum at 50° C