Nitrogen → 1-(2,2-Diethoxyethyl)cyclopropane

Temperatur

0 °C

Diazomethane (6.17 g, 147 mmol) was added dropwise to 3.02 g (21 mmol) of 3-butenal diethyl acetal in 10 ml of dry ether with intensive stirring at 0° C. Then 70 mg (0.312 mmol) of palladium (II) acetate in 50 ml of dry ether was added all at once. Then stirring at 0° C. continued until the evolution of N2 ceased (10 min.). The ether was distilled off to the reduced volume of the reaction mixture ca 10 ml. The precipitate was filtered off on a fritted glass funnel and the filtrate evaporated. The crude product (2.57 g) contained 97% of the title compound (GC) and was used without further purification.

1. stirringThen stirring at 0° C.
2. custom(10 min.)
3. distillationThe ether was distilled off to the reduced volume of the reaction mixture ca 10 ml
4. filtrationThe precipitate was filtered off on a fritted glass funnel
5. customthe filtrate evaporated
6. customwas used without further purification

ORD-Eintrag

ord-ac349e32008f4c8e8140cd83140d9543

Quelldatensatz

uspto-grants-2000_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06114365