تفاعل #1994268

معادلة التفاعل

benzyltrimethylammonium 1,1,3,3,3-pentafluoro-2-(3,7,12-trioxocholanoyloxy)-1-propanesulfonate

1-(2,2,2-trifluoroethoxy)naphthalene

tetramethylene sulfoxide

diisopropyl ether

→

4-(2,2,2-trifluoroethoxy)-1-naphthyl-tetrahydrothiophenium 1,1,3,3,3-pentafluoro-2-(3,7,12-trioxocholanoyloxy)-1-propanesulfonate

المردود 67.0%

المذيبات

water

Eaton's reagent

water

ظروف التفاعل

المعالجة

1. 1
   أخرىin Synthesis Example 1-3
2. 2
   أخرىwas separated
3. 3
   غسيلThe water layer was again washed with 30 g of diisopropyl ether
4. 4
   استخلاصafter which extraction
5. 5
   غسيلThe organic layer was washed with water
6. 6
   workup.DISTILLATIONdistilled in vacuum
7. 7
   أخرىto remove the solvent
8. 8
   أخرىpurified by silica gel column chromatography (elute, dichloromethane/methanol)
9. 9
   workup.DISSOLUTIONThe product was dissolved in methyl isobutyl ketone
10. 10
    غسيلwashed with water
11. 11
    workup.DISTILLATIONdistilled in vacuum
12. 12
    أخرىto remove the solvent
13. 13
    أخرىdried in vacuum
14. 14
    workup.ADDITIONThe product was poured into isopropyl ether for crystallization
15. 15
    ترشيحfiltered
16. 16
    أخرىdried
17. 17
    أخرىobtaining the target compound

الإجراء التجريبي

In 6 g of Eaton's reagent (Aldrich, diphosphorus pentoxide/methanesulfonic acid solution) was dispersed 3.4 g (0.0150 mol) of 1-(2,2,2-trifluoroethoxy)naphthalene in Synthesis Example 1-3. With stirring, 3.2 g (0.0300 mol) of tetramethylene sulfoxide was added dropwise to the dispersion. The solution was matured overnight at room temperature and combined with 30 g of water and 30 g of diisopropyl ether, from which a water layer was separated. The water layer was again washed with 30 g of diisopropyl ether. This aqueous solution was combined with 3.4 g (0.0100 mol) of benzyltrimethylammonium 1,1,3,3,3-pentafluoro-2-(3,7,12-trioxocholanoyloxy)-1-propanesulfonate in Synthesis Example 1-7, after which extraction was effected twice with 50 g of dichloromethane. The organic layer was washed with water, distilled in vacuum to remove the solvent, and purified by silica gel column chromatography (elute, dichloromethane/methanol). The product was dissolved in methyl isobutyl ketone, washed with water, distilled in vacuum to remove the solvent, and dried in vacuum. The product was poured into isopropyl ether for crystallization, filtered and dried, obtaining the target compound. White crystals, 6.2 g, yield 67%.

المصدر