反应详情

Under atmosphere of argon, to a suspension of sodium hydride (63%, 57.1 g) in anhydrous N,N-dimethylformamide (540 ml) was added a solution of 3,4-dihydroxybenzaldehyde (103.5 g) in anhydrous N,N-dimethylformamide (500 ml) dropwise slowly under cooling with ice. The reaction mixture was stirred for 30 minutes at room temperature, and to the mixture was added benzyl chloride (104 ml) under cooling with ice and it was stirred for 15 hours at room temperature. To the mixture was added water under cooling with ice, and was concentrated under reduced pressure. The residue was diluted by water and it was washed by methylene chloride. The methylene chloride layer was extracted by a 1N aqueous solution of sodium hydroxide. Combined aqueous layers were acidified by 2M hydrochloric acid and it was extracted by ethyl acetate. The organic layer was washed by a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate and concentrated. The residue was recrystallized from chloroform to give the title compound (99.4 g) having the following physical data.

1. temperatureunder cooling with ice
2. temperatureunder cooling with ice and it
3. stirringwas stirred for 15 hours at room temperature
4. temperatureunder cooling with ice
5. concentrationwas concentrated under reduced pressure
6. additionThe residue was diluted by water and it
7. washwas washed by methylene chloride
8. extractionThe methylene chloride layer was extracted by a 1N aqueous solution of sodium hydroxide
9. extractionwas extracted by ethyl acetate
10. washThe organic layer was washed by a saturated aqueous solution of sodium chloride
11. dry with materialdried over anhydrous sodium sulfate
12. concentrationconcentrated
13. customThe residue was recrystallized from chloroform