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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1439706Erstellt: 26. Oktober 2026

Acetic Acid → Diethyl 3-ethyl-1,3-dihydro-2H-pyrrole-2,2-dicarboxylate

https://huagongshe.com/reaction/1439706

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2-PentenalHCID 12993—
EduktDiethyl 2-(benzyloxycarbonylamino)malonateHCID 259787—
EduktSodiumHCID 5360545—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
ProduktDiethyl 3-ethyl-1,3-dihydro-2H-pyrrole-2,2-dicarboxylateHCID 2186630063%

Reaktionsschritte

Diethyl benzyloxycarbonylaminomalonate (11.5 g, 38 mM) was dissolved in dry ethanol (50 ml) and added to a solution of sodium (150 mg) in dry ethanol (10 ml). Pent-2-enal (3.2 g 38 mM) in ethanol (10 ml) was added dropwise to the stirred mixture and the solution stirred for 1 hr. A solution of acetic acid (0.29 ml) in ethanol (1 ml) was then added and the solution hydrogenated for 2 hrs at atmospheric pressure using palladium on carbon (5%) as catalyst. The catalyst was removed by filtration and the filtrate evaporated. The residue was dissolved in chloroform and the solution washed with brine containing a little sodium bicarbonate, dried (Na2SO4) and evaporated. Distillation of the residue at 15 mm Hg gave 4-ethyl-5,5-dicarboethoxy-2-pyrroline (5.65 g) as a colourless oil b.p. 115°-120° (15 mm Hg) I.R. 1715, 1610 cm-1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04060603
Quelldatensatzuspto-grants-1977_11
ORD IDord-164814b4299a4fe7828b0c9496c9c3ae
Quellennotizuspto-grants-1977_11