反应详情

温度

-78 °C

In a flame dried 20 mL vial was placed 6-bromo-2-methylene-2,3-dihydro-1H-inden-1-one (98 mg, 0.441 mmol) and it was dissolved in dichloromethane (4.5 mL). To this solution was added 2-trimethylsilyloxy-1,3-butadiene (98 μL, 0.565 mmol) and the solution was cooled down to −78° C. After stirring for 5 minutes, BF3.OEt2 (27 mL, 0.219 mmol) was slowly added. After 5 minutes of the BF3.OEt2 addition, TLC indicated consumption of the dienophile. The reaction was quenched with MeOH (300 μL), allowed to stir for 5 minutes at −78° C. and then warmed up to room temperature. Once at room temperature, 2M HCl (7 mL) was added. The phases were separated and the aqueous phase was back-extracted with dichloromethane twice (5 mL/each). The combined organic phases were dried over MgSO4, filtered and concentrated under reduce pressure. The crude material was purified by flash chromatography (ISCO, 12 g SiO2 cartridge, ethyl acetate/hexanes as the eluents). The corresponding fractions were combined and concentrated under reduce pressure yielding 6′-bromospiro[cyclohexane-1,2′-indene]-1′,4(3′H)-dione (62 mg, 0.212 mmol, 48% yield).

1. customIn a flame dried 20 mL
2. customconsumption of the dienophile
3. customThe reaction was quenched with MeOH (300 μL)
4. stirringto stir for 5 minutes at −78° C.
5. temperaturewarmed up to room temperature
6. additionOnce at room temperature, 2M HCl (7 mL) was added
7. customThe phases were separated
8. extractionthe aqueous phase was back-extracted with dichloromethane twice (5 mL/each)
9. dry with materialThe combined organic phases were dried over MgSO4
10. filtrationfiltered
11. concentrationconcentrated
12. customThe crude material was purified by flash chromatography (ISCO, 12 g SiO2 cartridge, ethyl acetate/hexanes as the eluents)
13. concentrationconcentrated