反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- temperatureThe mixture was then heated to 60°-65° C. at pH 8.0
- customthe aqueous phase separated
- temperatureslowly heated
- additionafter the addition of 0.4 g finely granulated sodium hydroxide at 70° C
- customproduced during the reaction
- customwas separated from 70°-100° C
- additionwas added
- customthe aqueous phase separated
- temperaturewarm water which
- customwas separated again after a brief agitation at 65° C
- distillationAfter distilling the organic phase on a water separator the phase
- concentrationwas concentrated to 120 ml
- filtrationfiltered hot
- temperatureslowly cooled off under agitation, during which the product
- customseparated in colorless crystals
- filtrationThese crystals were filtered off after 30 min agitation at 5° C.
- washwashed with cold toluene
- customdried in a vacuum at 50° C