反应详情

2,2,6,6-Tetramethylbenzo[1,2-d:4,5-d']bis(1,3)dioxole (8.80 g, 40.00 mmol, Example 5) was dissolved in THF (100 mL) and cooled to -20° C. n-Butyllithium (25.0 mL, 40.0 mmol, 1.6M) was added and the temperature was adjusted to ambient temperature over a period of 30 minutes and then recooled to -20° C. Bis(2,2,6,6-tetramethylbenzo-(1,2-d:4,5-d']bis(1,3)dioxole-4-yl)ketone (18.80 g, 39.83 mmol, Example 57) was added and the temperature was once more adjusted to room temperature and the mixture was stirred for 18 hours. The mixture was then poured on water/AcOH (100 mL, 2% AcOH) and extracted with diethyl ether (2×100 mL). The organic phase was washed with water (2×100 ml) and dried (Na2SO4). The solvent was evaporated and the product was washed with petroleum ether (20 mL, 40-60° C.). Yield 10.80 g (64.1%). Spectral data see example 44.

1. additionwas added
2. customrecooled to -20° C
3. customwas once more adjusted to room temperature
4. additionThe mixture was then poured on water/AcOH (100 mL, 2% AcOH)
5. extractionextracted with diethyl ether (2×100 mL)
6. washThe organic phase was washed with water (2×100 ml)
7. dry with materialdried (Na2SO4)
8. customThe solvent was evaporated
9. washthe product was washed with petroleum ether (20 mL, 40-60° C.)