HRID434846

反应详情

EQUATION

反应方程式

HRID 434846 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

5-(2-Chloro-6-methoxyphenyl)oxazolidin-2,4-dione (1.21 g., 5 mmoles) was suspended in 25 ml. of 1,2-dichloroethane. Triethylamine (1 drop) and then methyl isocyanate (285 mg., 0.29 ml., 5 mmoles) were added and the mixture stirred for 3 hours at room temperature, by which time solution had resulted. The reaction mixture was diluted with 50 ml. of 1,2-dichloroethane, washed with two portions of saturated sodium bicarbonate and then with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to product. Recrystallization from chloroform-hexane afforded purified 5-(2-chloro-6-methoxyphenyl)-3-methylcarbamoyloxazolidin-2,4-dione [1.04 g., 70%; m.p. 124°-127° C. (dec); m/e 300/298].

WORKUP

后处理

  1. customhad resulted
  2. additionThe reaction mixture was diluted with 50 ml
  3. washof 1,2-dichloroethane, washed with two portions of saturated sodium bicarbonate
  4. dry with materialwith brine, dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated to product
  7. customRecrystallization from chloroform-hexane
  8. customafforded
  9. custompurified 5-(2-chloro-6-methoxyphenyl)-3-methylcarbamoyloxazolidin-2,4-dione [1.04 g., 70%; m.p. 124°-127° C. (dec); m/e 300/298]