反应详情

温度

0 °C

At 0° C. and under argon, 343.4 mg (0.64 mmol) of 2-(benzyloxy)benzyl-triphenylphosphonium bromide from Ex. III are suspended in 20 ml of THF, and 0.48 ml of butyllithium (0.76 mmol, 1.6 M solution in hexane) is added. The deep-orange solution is stirred at 0° C. for 30 min, and a solution of 195 mg (0.64 mmol) of methyl 6-formyl-7-(4-methoxycarbonylphenyl)heptanoate (prepared analogously to Example I from t-butyl 2-oxocyclohexanecarboxylate and methyl 4-chloromethylbenzoate, cf. EP-A-0 341 551) in 15 ml of THF is added dropwise at this temperature. The mixture is stirred at 0° C. for 30 min. At 0° C., water is added, and the mixture is then warmed to room temperature and extracted with ethyl acetate. The organic phase is washed with sodium chloride solution, dried with magnesium sulfate and concentrated using a rotary evaporator. For purification, the substance was chromatographed on 40 g of silica gel 60 (particle size 0.040-0.063 mm) using the mobile phase petroleum ether/ether 4:1 to 1:1.

1. customAt 0° C.
2. stirringThe mixture is stirred at 0° C. for 30 min
3. temperaturethe mixture is then warmed to room temperature
4. extractionextracted with ethyl acetate
5. washThe organic phase is washed with sodium chloride solution
6. dry with materialdried with magnesium sulfate
7. concentrationconcentrated
8. customa rotary evaporator
9. customFor purification
10. customthe substance was chromatographed on 40 g of silica gel 60 (particle size 0.040-0.063 mm)