Réaction #1960495
ord-2fd8d632df444939aeb159f484faf82f
Équation de réaction
Réactifs
Aucun
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1workup.ADDITIONare added over the course of 20 min with ice-
- 2Températurecooling
- 3Extractionthe mixture is extracted a number of times with MTBE
- 4LavageThe combined organic phases are washed with water and saturated sodium chloride soln
- 5Autre, and the solution is dried
- 6Autreafter removal of the solvents
- 7Autreis purified by column chromatography (SiO2, n-heptane:MTBE=2:1)
Mode opératoire
10.0 g (39.0 mmol) of 7,8-difluoro-2-pentylchroman-6-ol are initially introduced in 140 ml of THF together with 4.0 g (41.0 mmol) of 1-hexyn-3-ol and 11.3 g (42.9 mmol) of triphenylphosphine, and 9.1 ml (46.8 mmol) of DIAD are added over the course of 20 min with ice-cooling. After 18 h at RT, water 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 soln., and the solution is dried using sodium sulfate. The residue remaining after removal of the solvents is purified by column chromatography (SiO2, n-heptane:MTBE=2:1), giving 6-(1-ethynylbutoxy)-7,8-difluoro-2-pentylchroman as a yellow oil.