反应详情

A flask charged with a stir bar, 1-bromo-4-(2,3,4,6-tetra-O-acetyl-D-glucopyranos-1-yl)-2-(phenoxymethyl)-benzene (14.7 g), copper cyanide (4.1 g), and NMP (100 mL) is heated at reflux temperature for 8 h. After dilution with water (600 mL), the precipitate is separated, washed a few times with water and subsequently dissolved in ethyl acetate (200 mL). The resultant solution is filtered through a plug of silica gel using ethyl acetate (300 mL) as the eluent. The filtrate is concentrated under reduced pressure and the residue is dissolved in dichloromethane (100 mL) to reacetylate the oxygen groups deprotected during the cyanation. Accordingly, pyridine (4 mL), 4-dimethylaminopyridine (0.3 g) and acetic anhydride (4.4 mL) are added in succession. The resulting solution is stirred at room temperature for 1 h. Then, the reaction mixture is diluted with dichloromethane (50 mL) and washed thrice with 1 M aqueous hydrochloric acid, once with aqueous sodium hydrogen carbonate solution and once with water. The organic phase is dried (sodium sulphate) and the solvent is removed. The residue is recrystallized from ethanol.

1. additionA flask charged with a stir bar
2. temperatureat reflux temperature for 8 h
3. customAfter dilution with water (600 mL), the precipitate is separated
4. washwashed a few times with water
5. dissolutionsubsequently dissolved in ethyl acetate (200 mL)
6. filtrationThe resultant solution is filtered through a plug of silica gel
7. concentrationThe filtrate is concentrated under reduced pressure
8. dissolutionthe residue is dissolved in dichloromethane (100 mL)
9. additionAccordingly, pyridine (4 mL), 4-dimethylaminopyridine (0.3 g) and acetic anhydride (4.4 mL) are added in succession
10. additionThen, the reaction mixture is diluted with dichloromethane (50 mL)
11. washwashed thrice with 1 M aqueous hydrochloric acid
12. dry with materialThe organic phase is dried (sodium sulphate)
13. customthe solvent is removed
14. customThe residue is recrystallized from ethanol