反应详情

To a solution of 4-(4-phenylbutylidene)-1-benzylpiperidine from Step C (4.37 g) in anhydrous ether (150 mL) under nitrogen with stirring was add 1M borane solution in THF (45 mL). The reaction was stirred for 3 h when water (2 mL) was added dropwise. The mixture was stirred a further 30 min and was then cooled in an ice bath. A solution of chromic anhydride (2.5 g), concentrated sulfuric acid (5.44 mL) and water (125 mL) was added dropwise with vigorous magnetic stirring over 5 min. After another 5 min, the ice bath was removed. After 1.5 h at rt, 0.5N sodium hydroxide and ether (400 mL each) were added and the mixture was stirred until the residue dissolved. The layers were separated and the aqueous layer was extracted twice with ether. The combined ether layers were washed with an aqueous EDTA solution, water and brine (100 mL each), dried over sodium sulfate and concentrated under reduced-pressure to give a colorless gel. Flash chromatography on silica gel with 30-50% ethyl acetate in hexanes with 3% (v/v) TEA gave the title compound (1 g) as a colorless gel. Rf: 0.43 (30% ethyl acetate in hexanes with 3% (v/v) TEA).

1. additionwas added dropwise
2. temperaturewas then cooled in an ice bath
3. stirringmagnetic stirring over 5 min
4. waitAfter another 5 min
5. customthe ice bath was removed
6. waitAfter 1.5 h at rt
7. addition0.5N sodium hydroxide and ether (400 mL each) were added
8. stirringthe mixture was stirred until the residue
9. dissolutiondissolved
10. customThe layers were separated
11. extractionthe aqueous layer was extracted twice with ether
12. washThe combined ether layers were washed with an aqueous EDTA solution, water and brine (100 mL each)
13. dry with materialdried over sodium sulfate
14. concentrationconcentrated under reduced-pressure
15. customto give a colorless gel