反应详情

温度

-78 °C

Diisopropylamine (3.14 g, 4.38 mL, 31.0 mmol) was dissolved in THF (100 mL) and cooled to −78° C. To this solution was added 2.5 M n-butyl lithium in hexane (12.4 mL, 31.0 mmol) and stirred for 15 min, warmed up to 0° C. and stirred for an additional min, then re-cooled to −78° C. 4-(tert-Butyl-diphenyl-silanyloxy)-cyclohexanecarboxylic acid ethyl ester (10.5 g, 25.6 mmol) in THF (15 mL) was then added and the reaction mixture was allowed to stir at −78° C. for 1.0 h followed by the addition of a mixture of hexamethyl-phosphoramide (HMPA) (7 mL) and allyl iodide (5.59 g, 33.3.0 mmol). This mixture was stirred at −78° C. for 20 min. Then, the dry ice bath was removed and the stirring was continued to allow the reaction mixture to warm to room temperature over 1 h. The reaction mixture was poured into ice-water (100 mL) and ether (50 mL). The two layers were separated; the aqueous layer was extracted with ether (3×50 mL). The combined organic layers were washed with brine, dried over Na2SO4, and concentrated under vacuum to afford 11.4 g (99%) of the title compound.

1. temperaturewarmed up to 0° C.
2. stirringstirred for an additional min
3. temperaturere-cooled to −78° C
4. stirringto stir at −78° C. for 1.0 h
5. stirringThis mixture was stirred at −78° C. for 20 min
6. customThen, the dry ice bath was removed
7. temperatureto warm to room temperature over 1 h
8. additionThe reaction mixture was poured into ice-water (100 mL) and ether (50 mL)
9. customThe two layers were separated
10. extractionthe aqueous layer was extracted with ether (3×50 mL)
11. washThe combined organic layers were washed with brine
12. dry with materialdried over Na2SO4
13. concentrationconcentrated under vacuum