Réaction #2692
ord-20a28c547f764190864154877d314000
Équation de réaction
Réactifs
Réactifs
Conditions de réaction
Traitement
- 1workup.ADDITIONfilled
- 2Autrereaction flask
- 3workup.STIRRINGafter stirring overnight
- 4Filtrationthe ether was filtered off
- 5LavageThe solid residue was washed with chloroform
- 6Autredried under vacuum
- 7workup.STIRRINGwas stirred for 1.5 h at 60° C
- 8workup.WAITThe stirring was continued overnight
- 9FiltrationThe mixture was filtered
- 10Autrethe solution evaporated
- 11workup.DISSOLUTIONthe residue was dissolved in dichloromethane
- 12LavageThe organic phase was washed with water (2*30 mL)
- 13Séchagedried (Na2SO4)
- 14Autreevaporated
- 15Autreto give
- 16Autreafter additional drying under vacuum a bright green-yellow crystalline pure product
Mode opératoire
2,2,6,6-Tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole (2.0 g, 6.98 mmol) was dissolved in dry ether (50.0 mL) in a dry, argon filled reaction flask. n-Butyllithium (3.07 mL, 2.5M in hexane) was added and the reaction mixture was stirred for 30 min. The solution was poured onto solid carbon dioxide and, after stirring overnight, the ether was filtered off. The solid residue was washed with chloroform and dried under vacuum. The crude product was mixed with potassium carbonate (0.97 g, 6.98 mmol) in dry DMF (20.0 mL) and was stirred for 1.5 h at 60° C. After cooling to ambient temperature, methyl iodide (0.435 mL, 6.98 mmol) was added. The stirring was continued overnight. The mixture was filtered, the solution evaporated and the residue was dissolved in dichloromethane and water. The organic phase was washed with water (2*30 mL), dried (Na2SO4) and evaporated to give after additional drying under vacuum a bright green-yellow crystalline pure product.