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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 328073Erstellt: 24. Oktober 2026

Water → Tert.-butyl 2-chloro-3-cyclopentyl-2,3-epoxy-butanoate

https://huagongshe.com/de/reaction/328073

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktHexaneHCID 8058—
EduktCyclopentyl methyl ketoneHCID 22326—
Edukt1,1-Dimethylethyl dichloroacetateHCID 3016483—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert.-butyl 2-chloro-3-cyclopentyl-2,3-epoxy-butanoateHCID 21443888—

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

A mixture of 12.3 g of cyclopentylmethyl ketone and 18.5 g of tert.-butyl dichloroacetate was cooled to -30° C with stirring under an inert atmosphere and a solution of 12.2 g of potassium tert.-butylate in 60 ml of tetrahydrofuran was added thereto at the said temperature. After returning to room temperature, hexane and water were added and the organic phase was separated, washed with water and dried over magnesium sulfate. The solvents were evaporated off to leave an oily residue of tert.-butyl 2-chloro-3-cyclopentyl-2,3-epoxy-butanoate. 26.5 g of the latter product was added to a solution of 3 g of lithium carbonate and 20 g of lithium bromide in 100 ml of hexamethylphosphorotriamide and after stirring for 1 hour at room temperature, petroleum ether and water were added thereto. The organic phase was washed with water, dried over magnesium sulfate and filtered. The solvent was evaporated to obtain an oily residue which was tert.-butyl 3-cyclopentyl-2-oxo-3-butenoate which was used as is for the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04016158
Quelldatensatzuspto-grants-1977_04
ORD IDord-5efebaedd46c470e8f15e08ae676c09b
Quellennotizuspto-grants-1977_04