反应详情

Under argon atmosphere, anhydrous THF (9 ml) was combined with Sm (1.01 g, 6.71 mmol), and then, at room temperature, 1,2-diiodoethane (1.05 g, 3.73 mmol) was added. The reaction solution was stirred for 1 hour at room temperature, and then cooled to −7 degrees C. to −2 degrees C., and 2-(2-chloro-2-propenyl)-5-(4-chlorobenzyl)-2-methylcyclopentanone (Compound (V), (Ra)Xana=CH3, (Rb)Xbnb=CH2CCl═CH2, Ym=4-Cl) dissolved in diiodomethane (0.90 g, 0.00168×2.0 mol) and THF (5 ml) was added, and stirred for 1.5 hours at the same temperature. To this, a 2N aqueous solution of NaOH (8 ml) was added, and stirring was conducted for 1 hour while cooling with ice. A 2N aqueous solution of hydrochloric acid (8 ml) was added, and then extraction with hexane (100 ml×2) was conducted. The organic layer was washed with water (50 ml) and saturated brine (30 ml), and then dried over anhydrous sodium sulfate and concentrated to obtain a crude intended substance (0.44 g), which was used in the next reaction as it was.

1. temperaturecooled to −7 degrees C
2. customto −2 degrees C
3. stirringstirred for 1.5 hours at the same temperature
4. stirringstirring
5. waitwas conducted for 1 hour
6. temperaturewhile cooling with ice
7. extractionextraction with hexane (100 ml×2)
8. washThe organic layer was washed with water (50 ml) and saturated brine (30 ml)
9. dry with materialdried over anhydrous sodium sulfate
10. concentrationconcentrated
11. customto obtain a crude
12. customwas used in the next reaction as it