Réaction #56590
ord-7f83b244a5014c8fbe2f48fda79a83a5
Équation de réaction
2-(6-chlorohexyloxy)tetrahydropyrane
hydroquinone
potassiumcarbonate
potassiumiodide
→
product
Rendement 82.5%
4-(6-(2-Tetrahydropyranyl)oxyhexyloxy)phenol
Rendement 82.5%
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Autreto react for 4 days at 80° C
- 2Extractionextracted with ether
- 3SéchageThe organic phase was then dried over sodium sulphate
- 4Filtrationfiltered
- 5Concentrationconcentrated to dryness
Mode opératoire
A mixture of 10 g of 2-(6-chlorohexyloxy)tetrahydropyrane, 25 g of hydroquinone, 31 g of potassiumcarbonate, 0.752 g of potassiumiodide and 250 ml of dimethylsulfoxide was allowed to react for 4 days at 80° C. Subsequently, the reaction mixture was cooled to room temperature and after addition of water extracted with ether. The organic phase was then dried over sodium sulphate, filtered and concentrated to dryness. Chromatography on silica with 10% ethylacetate in toluene gave 11 g of product as a yellowish oil.