反应详情

温度

0 °C

A solution of 7-chloro-1,3,4,5-tetrahydro-3-(methoxycarbonyl)-4-(4-methoxyphenyl)-2H-1-benzazepin-2-one (15 g, 41.7 mmole) in 780 ml of tetrahydrofuran was cooled to -78° C. and 147 ml (167 mmole in tetrahydrofuran) of potassium hexamethyldisilazide solution was added. After stirring for 1 hour, 28.7 ml of triethyl phosphite (166.7 mmole) was added and anhydrous oxygen gas was rapidly bubbled through the resulting solution. The reaction temperature was then raised to 0° C. and allowed to stir for an additional hour. Oxygenation was then discontinued and the reaction was quenched by the addition of 50 ml of acetic acid. The reaction mixture was then concentrated and the residue dissolved in ethyl acetate. The organic solution was washed successively with 1N hydrochloric acid, saturated sodium bicarbonate, and brine and then dried over anhydrous sodium sulfate. Concentration of the dried organic solution afforded a solid which, upon trituration in hexane, gave 14.8 g of the title compound.

1. customanhydrous oxygen gas was rapidly bubbled through the resulting solution
2. stirringto stir for an additional hour
3. customOxygenation
4. customthe reaction was quenched by the addition of 50 ml of acetic acid
5. concentrationThe reaction mixture was then concentrated
6. dissolutionthe residue dissolved in ethyl acetate
7. washThe organic solution was washed successively with 1N hydrochloric acid, saturated sodium bicarbonate, and brine
8. dry with materialdried over anhydrous sodium sulfate
9. customConcentration of the dried organic solution afforded a solid which