Réaction #2507820

Équation de réaction

n-butyllithium

n-butyllithium

p-toluenesulfonyl chloride

2-(6-fluoro-3-propylchroman-7-yl)propane-1,3-diol

→

6-Fluoro-7-oxetan-3-yl-3-propylchroman

Solvants

hexane

hexane

THF

THF

Conditions de réaction

Traitement

1. 1
   Températurere-cooled to 0° C
2. 2
   Autrethe cooling is removed
3. 3
   Températurethe batch is heated
4. 4
   Températureunder reflux for 4 h
5. 5
   workup.ADDITIONThe batch is subsequently diluted with MTB ether
6. 6
   Lavagewashed with water
7. 7
   Séchagephase is dried over sodium sulfate
8. 8
   Autreevaporated
9. 9
   Autrethe crude product is purified by chromatography on silica gel with heptane/ethyl acetate (3:2)
10. 10
    AutreThe product fractions (Rf=0.5) are evaporated
11. 11
    Autrethe product is used without further purification

Mode opératoire

3.80 g (13.7 mmol) of 2-(6-fluoro-3-propylchroman-7-yl)propane-1,3-diol are dissolved in 70 ml of THF, and 8.7 ml (13.7 mmol) of a 15 percent solution of n-butyllithium in hexane are added at 0° C. After 30 min, 2.7 g (14.2 mmol) of p-toluenesulfonyl chloride in 30 ml of THF are added, and the mixture is stirred at RT for 1 h and re-cooled to 0° C. After addition of a further 8.7 ml (13.7 mmol) of a 15% solution of n-butyllithium in hexane, the cooling is removed, and the batch is heated under reflux for 4 h. The batch is subsequently diluted with MTB ether and washed with water. The org. phase is dried over sodium sulfate and evaporated, and the crude product is purified by chromatography on silica gel with heptane/ethyl acetate (3:2). The product fractions (Rf=0.5) are evaporated, and the product is used without further purification.

Source