反应详情

A mixture of 23.199 g (62.85 mmole) 1-(t-butoxycarbonyl)-4-(2,2-dibromoethen-1-yl)piperidine (prepared as in Step B3 above) and 600 mL anhydrous THF was cooled with dry ice acetone bath under nitrogen. To this mixture was added 88 mL of a 1.6 M butyl lithium solution in hexanes dropwise with stirring and cooling over 50 minutes. After one hour, the flask was transferred into an ice bath. After another hour, a solution of 28.64 g (87.99 mmole) tributyltin chloride in 100 mL THF was added with stirring and cooling over 35 minutes. After three h, the mixture was concentrated under vacuum to remove some THF, and the residue was partitioned between 600 mL ice water and 800 mL ether. The organic layer was washed with 200 mL of water (1×), 2% sodium bicarbonate (1×), water (2×), and saturated brine (1×), dried over sodium sulfate and concentrated under vacuum to give 30.104 g crude product as a green-yellowish liquid. FC on 275 g silica gel using cold 2.5˜15% ethyl acetate in hexanes as quickly as possible to give 27.115 g title compound as a colorless liquid.

1. temperaturewas cooled with dry ice acetone bath under nitrogen
2. temperaturecooling over 50 minutes
3. customthe flask was transferred into an ice bath
4. waitAfter another hour
5. stirringwith stirring
6. temperaturecooling over 35 minutes
7. concentrationAfter three h, the mixture was concentrated under vacuum
8. customto remove some THF
9. customthe residue was partitioned between 600 mL ice water and 800 mL ether
10. washThe organic layer was washed with 200 mL of water (1×), 2% sodium bicarbonate (1×), water (2×), and saturated brine (1×)
11. dry with materialdried over sodium sulfate
12. concentrationconcentrated under vacuum
13. customto give 30.104 g crude product as a green-yellowish liquid