反应详情

To a mixture of 0.650 g. (16.91 mmole) of sodium borohydride and 3.17 g. (45.2 mmoles) of 2-methyl-2-butene in 40 ml. of diglyme cooled to -5° C. under an inert atmosphere is added over 15 minutes 3.24 g. (22.6 mmoles) of boron trifluoride etherate and the resulting mixture is stirred at 0° C. for 2 hours. To this mixture is then added over 5 minutes 8.32 g. (22.6 mmoles) of 3-triphenylmethoxyl-1-octyne (Example 127) in 10 ml. diglyme, the cooling bath is removed, and the mixture is stirred at ambient temperature for 1.5 hours. The mixture is cooled to 0° C. and 6.0 g. of finely divided anhydrous trimethylamine oxide is added over 10 minutes. The cooling bath is removed and the mixture is stirred at ambient temperatures for 0.5 hour. The mixture is then poured into 200 ml. of 15 % sodium hydroxide solution, a solution of 16 g. (63 mmoles) of iodine in 20 ml. of tetrahydrofuran is added immediately, and the resulting mixture is stirred for 0.5 hour. The organic phase is separated and the aqueous phase is washed with ether. The combined organic phase and washings are decolorized with 5% sodium thiosulfate solution, washed with saturated brine, dried (Na2SO4), and evaporated. The residue is dry-columned chromatographed upon alumina using hexane as eluent and the title compound is isolated as an oil.

1. additionTo a mixture of 0.650 g
2. additionis added over 15 minutes 3.24 g
3. additionTo this mixture is then added over 5 minutes 8.32 g
4. customdiglyme, the cooling bath is removed
5. temperatureThe mixture is cooled to 0° C.
6. additionof finely divided anhydrous trimethylamine oxide is added over 10 minutes
7. customThe cooling bath is removed
8. stirringthe mixture is stirred at ambient temperatures for 0.5 hour
9. additionThe mixture is then poured into 200 ml
10. stirringthe resulting mixture is stirred for 0.5 hour
11. customThe organic phase is separated
12. washthe aqueous phase is washed with ether
13. washwashed with saturated brine
14. dry with materialdried (Na2SO4)
15. customevaporated
16. customThe residue is dry-columned chromatographed upon alumina