HRID127771

反应详情

EQUATION

反应方程式

HRID 127771 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

6.1 G. (35.5 mmol) of 2,4-dimethyl-3-hydroxymethyl-5-methoxythiophene were added at 35° C. with vigorous stirring to a suspension of 13.4 g. (39.0 mmol) of triphenylphosphonium bromide in 250 ml. of acetonitrile. The deep purple color which was formed immediately, disappeared after some minutes. The reaction mixture was stirred for 3 hrs. The solvent was evaporated to a volume of about 25 ml. and an excess of cold ether was added. The solvent then was decanted from the resulting oily precipitate which was dissolved in warm acetone and again precipitated by adding cold ether. The solvent was decanted and the resulting oily residue was dried in high vacuum to yield (2,4-dimethyl-5-methoxy-3-thenyl)triphenylphosphonium bromide.

WORKUP

后处理

  1. customThe deep purple color which was formed immediately
  2. waitdisappeared after some minutes
  3. stirringThe reaction mixture was stirred for 3 hrs
  4. customThe solvent was evaporated to a volume of about 25 ml
  5. additionand an excess of cold ether was added
  6. customThe solvent then was decanted from the resulting oily precipitate which
  7. dissolutionwas dissolved in warm acetone
  8. customagain precipitated
  9. additionby adding cold ether
  10. customThe solvent was decanted
  11. customthe resulting oily residue was dried in high vacuum