HRID1109356

反应详情

EQUATION

反应方程式

HRID 1109356 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

5-(3,5-Di-tert-butyl-4-hydroxybenzylidene)thiazolidin-4-one (479 mg, 1.5 mmole) described in Kokai 62-42977 was suspended in dried toluene (3 ml), to which chlorosulfonyl isocyanate (144 μl; 1.65 mmole) was added with stirring under nitrogen atmosphere, to obtain a transparent solution of orange color. Furthermore, the solution was heated at 90° C. for 10 min., from which toluene was evaporated under reduced pressure, then 3.6 ml of mixed solution of acetic acid and water (2:1) was added thereto. The resulting mixture was heated at 90° C. for 10 min. and poured into ice-water, which was subjected to extraction with dichloromethane. The obtained organic layer was washed with water and saturated brine, dried over magnesium sulfate, and evaporated. The obtained residue was separated by using silica gel chromatography (chloroform:acetone=20:1), whereby 377 mg of the objective compound was obtained, which was recrystallized from ethanol-ether in 53% yield. The physical constants are described on Table 1.

WORKUP

后处理

  1. additionwas added
  2. customto obtain a transparent solution of orange color
  3. customwas evaporated under reduced pressure
  4. addition3.6 ml of mixed solution of acetic acid and water (2:1) was added
  5. additionpoured into ice-water, which
  6. extractionwas subjected to extraction with dichloromethane
  7. washThe obtained organic layer was washed with water and saturated brine
  8. dry with materialdried over magnesium sulfate
  9. customevaporated
  10. customThe obtained residue was separated