HRID436108

反应详情

EQUATION

反应方程式

HRID 436108 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To 233 ml. of a 0.43M solution of disiamylborane in diglyme cooled to 0° C. under an inert atmosphere is added 23.8 g. (0.100 mole) 4,4-dimethyl-3-tetrahydropyranyloxy-1-octyne (Example 995). The mixture is allowed to come to room temperature and is stirred at ambient temperature for 3 hours. The solution is cooled to 0° C. and 22.5 g. (0.30 mole) of triethylamine oxide is added portionwise such that the temperature is maintained at 0°-5° C. The mixture is stirred at 0° C. for 1 hour and is then poured into 150 ml. of 1 N sodium hydroxide followed immediately by a solution of 25.4 g. (0.100 mole) of iodine in 60 ml. of tetrahydrofuran. The mixture is stirred at ambient temperatures for 0.5 hour and poured into 500 ml. of water. The mixture is decolorized by addition of sodium thiosulfate solution and is extracted into ether. The organic phase is washed with water and the solvent is removed in vacuo. The residue is stirred at room temperature for 20 hours with 900 ml. 3:1:1 tetrahydrofuran-acetic acid-water. The solution is evaporated in vacuo and the residue is chromatographed on silica gel in benzene using 10-20% ethylacetate in benzene.

WORKUP

后处理

  1. additionis added 23.8 g
  2. customto come to room temperature
  3. temperatureThe solution is cooled to 0° C.
  4. temperatureis maintained at 0°-5° C
  5. stirringThe mixture is stirred at 0° C. for 1 hour
  6. additionis then poured into 150 ml
  7. stirringThe mixture is stirred at ambient temperatures for 0.5 hour
  8. additionpoured into 500 ml
  9. extractionis extracted into ether
  10. washThe organic phase is washed with water
  11. customthe solvent is removed in vacuo
  12. stirringThe residue is stirred at room temperature for 20 hours with 900 ml
  13. customThe solution is evaporated in vacuo
  14. customthe residue is chromatographed on silica gel in benzene using 10-20% ethylacetate in benzene