反应详情

温度

-72 °C

6.9 g (36.34 mmol, 1 eq., 96% a % by GC) 1-allyl-cyclopropanecarboxylic acid tert-butyl ester were dissolved in 40 ml CH2Cl2 and 40 ml MeOH. The solution was cooled to −72° C. and the ozone was bubbled through the reaction mixture until a blue color was obtained. Then nitrogen was bubbled to remove excess ozone until a colorless solution was obtained. 10 ml (3.68 eq.) dimethyl sulfide and 14 ml (2.76 eq.) triethylamine were added. The reaction mixture was warmed to RT and stirred overnight at that temperature (peroxide test negative, pH 7-8). The yellowish reaction mixture was added to 100 ml sat. aq. ammonium chloride solution (exothermic) and extracted 3 times with 70 ml CH2Cl2. The organic phases were combined, dried over sodium sulfate, filtered and concentrated under reduced pressure to provide the crude aldehyde, which was purified by filtration over SiO2 (CH2Cl2; TLC:EtOAc/heptane 1:2) to provide 3.90 g (96% GC, 56% yield) of the title compound as an oil.

1. customthe ozone was bubbled through the reaction mixture until a blue color
2. customwas obtained
3. customThen nitrogen was bubbled
4. customto remove excess ozone until a colorless solution
5. customwas obtained
6. temperatureThe reaction mixture was warmed to RT
7. customThe yellowish reaction mixture
8. extractionextracted 3 times with 70 ml CH2Cl2
9. dry with materialdried over sodium sulfate
10. filtrationfiltered
11. concentrationconcentrated under reduced pressure
12. customto provide the crude aldehyde, which
13. filtrationwas purified by filtration over SiO2 (CH2Cl2; TLC:EtOAc/heptane 1:2)