反应详情

温度

-78 °C

To a solution of 1-bromonaphthalene (10 g, 48 mmol) in THF (100 ml), a 1.65 M solution of n-butyl lithium in n-hexane (58 ml, 96 mmol of n-butyl lithium) and stirred at -78° C. for one hour. Then, trimethoxyborane (10 g, 96 mmol) was added, and the mixture was stirred at -78° C. for 30 minutes, and then at room temperature for one hour. To the mixture, phenothiazine (132 mg) and then a mixture of conc. hydrochloric acid (20 ml), phosphoric acid (30 ml) and water (220 ml) were gradually added. After heating the mixture to room temperature and stirring it for 20 hours, the organic layer was separated. The aqueous solution was washed with diethyl ether. The combined organic layer was washed with a 10% aqueous solution of sodium chloride. To the ice-cooled organic layer, a 5% aqueous solution of sodium hydroxide was added and stirred. Then, the mixture was phase separated, and the aqueous layer was saturated with sodium chloride, acidified with phosphoric acid, and extracted with diethyl ether. The diethyl ether layer was dried over anhydrous magnesium sulfate. The solvent was evaporated off, and the obtained solid residue was recrystallized from ethyl acetate/n-hexane to obtain naphthylboric acid (4.20 g).

1. waitat room temperature for one hour
2. additionwere gradually added
3. temperatureAfter heating the mixture to room temperature
4. stirringstirring it for 20 hours
5. customthe organic layer was separated
6. washThe aqueous solution was washed with diethyl ether
7. washThe combined organic layer was washed with a 10% aqueous solution of sodium chloride
8. temperatureTo the ice-cooled organic layer
9. additiona 5% aqueous solution of sodium hydroxide was added
10. stirringstirred
11. customseparated
12. extractionextracted with diethyl ether
13. dry with materialThe diethyl ether layer was dried over anhydrous magnesium sulfate
14. customThe solvent was evaporated off
15. customthe obtained solid residue was recrystallized from ethyl acetate/n-hexane