反应详情

To a solution of 18.92 g (82.6 mmol) of 4-bromo-2-t-butylphenol (Compound E) in 110 ml of dichloromethane was added dropwise 10.42 g (11.3 ml, 123.9 mmol) of 3,4-dihydro-2H-pyran (DHP). To this clear, colorless solution was added 1.86 g (7.4 mmol) of pyridinium p-toluenesulfonate (PPTS). The resulting mixture was stirred at room temperature under a blanket of argon for 26.5 hours, partitioned between 250 ml of water and 400 ml of hexane, and the layers were separated. The organic phase was washed with 2×250 ml-portions of water and with 150 ml of brine solution, dried over MgSO4, filtered and concentrated in vacuo to a yellow oil. Purification by flash chromatography (silica, 5% ethyl acetate in hexane) yielded the title compound as a light yellow, crystalline solid. PMR (CDCl3): d 1.39 (9H, s), 1.6-2.1 (6H, m), 3.6-3.7 (1H, m), 3.8-3.9 (1H, m), 5.43 (1H, t, J=2.7 Hz), 7.06 (1H, d, J=8.8 Hz), 7.24 (1H, dd, J=8.8, 2.7 Hz), 7.36 (1H, d, J=2.7 Hz).

1. custompartitioned between 250 ml of water and 400 ml of hexane
2. customthe layers were separated
3. washThe organic phase was washed with 2×250 ml-portions of water and with 150 ml of brine solution
4. dry with materialdried over MgSO4
5. filtrationfiltered
6. concentrationconcentrated in vacuo to a yellow oil
7. customPurification by flash chromatography (silica, 5% ethyl acetate in hexane)