تفاعل #2692

معادلة التفاعل

carbon dioxide

methyl iodide

potassium carbonate

n-Butyllithium

2,2,6,6-Tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole

→

4-Methoxycarbonyl-(2,2,6,6-tetramethylbenzo[1,2-d:4,5-d']-bis(1,3)dithiole)

المذيبات

DMF

ether

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITIONfilled
2. 2
   أخرىreaction flask
3. 3
   workup.STIRRINGafter stirring overnight
4. 4
   ترشيحthe ether was filtered off
5. 5
   غسيلThe solid residue was washed with chloroform
6. 6
   أخرىdried under vacuum
7. 7
   workup.STIRRINGwas stirred for 1.5 h at 60° C
8. 8
   workup.WAITThe stirring was continued overnight
9. 9
   ترشيحThe mixture was filtered
10. 10
    أخرىthe solution evaporated
11. 11
    workup.DISSOLUTIONthe residue was dissolved in dichloromethane
12. 12
    غسيلThe organic phase was washed with water (2*30 mL)
13. 13
    تجفيفdried (Na2SO4)
14. 14
    أخرىevaporated
15. 15
    أخرىto give
16. 16
    أخرىafter additional drying under vacuum a bright green-yellow crystalline pure product

الإجراء التجريبي

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.

المصدر