Réaction #1960493

Équation de réaction

7,8-difluoro-2-pentylchroman-6-ol

1-(4-propylcyclohexyl)prop-2-yn-1-ol

triphenylphosphine

DIAD

sodium chloride

→

7,8-difluoro-2-pentyl-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]chroman

Solvants

THF

Conditions de réaction

Traitement

1. 1
   workup.ADDITIONare added over the course of 30 min with ice-
2. 2
   Températurecooling
3. 3
   Extractionthe mixture is extracted a number of times with MTBE
4. 4
   LavageThe combined organic phases are washed with water and saturated sodium chloride solution
5. 5
   Autrethe solution is dried
6. 6
   Autreafter removal of the solvents
7. 7
   Autreis purified by column chromatography (SiO2, n-pentane:MTBE=2:1)

Mode opératoire

8.0 g (31.2 mmol) of 7,8-difluoro-2-pentylchroman-6-ol are initially introduced in 75 ml of THF together with 6.75 g (37.4 mmol) of 1-(4-propylcyclohexyl)prop-2-yn-1-ol and 9.83 g (37.6 mmol) of triphenylphosphine, and 7.89 ml (40.6 mmol) of DIAD are added over the course of 30 min with ice-cooling. After 20 h at RT, semi-saturated sodium chloride solution is added, and the mixture is extracted a number of times with MTBE. The combined organic phases are washed with water and saturated sodium chloride solution, and the solution is dried using sodium sulfate. The residue remaining after removal of the solvents is purified by column chromatography (SiO2, n-pentane:MTBE=2:1), giving 7,8-difluoro-2-pentyl-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]chroman as a pale-brown oil.

Source