HRID1584295

反应详情

EQUATION

反应方程式

HRID 1584295 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 5-[3-methoxy-4-(2-phenyl-4-oxazolyl-methoxy)cinnamylidene]-2,4-oxazolidinedione (1.0 g), platinum oxide (PtO2) (0.2 g) and tetrahydrofuran (THF)-acetic acid (4:1, 190 ml) was subjected to catalytic hydrogenation under 1 atmospheric pressure at room temperature. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The concentrate was dissolved in chloroform, which was washed with water, a saturated aqueous solution of sodium hydrogencarbonate and water, successively, followed by drying (MgSO4). The chloroform layer was concentrated under reduced pressure, and the concentrate was subjected column chromatography on silica gel. From the fraction eluted with chloroform-ethyl acetate (4:1), 5-[3-[3-methoxy-4-(2-phenyl-4-oxazolylmethoxy)phenyl]propyl]-2,4-oxazolidinedione (0.19 g, 19%) was obtained. Recrystallization of the product from ethyl acetate-hexane gave colorless prisms, m.p.134-135° C.

WORKUP

后处理

  1. customwas subjected to catalytic hydrogenation under 1 atmospheric pressure at room temperature
  2. filtrationThe catalyst was filtered off
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. dissolutionThe concentrate was dissolved in chloroform
  5. washwhich was washed with water
  6. dry with materialby drying (MgSO4)
  7. concentrationThe chloroform layer was concentrated under reduced pressure
  8. washFrom the fraction eluted with chloroform-ethyl acetate (4:1)