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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36373Erstellt: 24. Oktober 2026

Potassium Hydroxide → Ethyl 2-benzylacrylate

https://huagongshe.com/de/reaction/36373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktDiethyl 2-benzylpropanedioateHCID 69090—
LösungsmittelEthanolHCID 702—
ProduktEthyl 2-benzylacrylateHCID 1108464885,5%

Reaktionsschritte

A mixture of of KOH (8.5 g) in ethanol (100 mL) was added at room temperature to benzylmalonic acid diethyl ester (40 g) in ethanol (80 mL) and the solution was stirred at room temperature overnight, then concentrated by evaporation. Water (14 mL) was added and then the mixture was acidified in an ice bath with concentrated hydrochloric acid (12.6 mL). The mixture was partitioned between water and ether; the organic phase was separated, dried and the ether was evaporated. The residue was treated with pyridine (26 mL), piperidine (1.22 g) and paraformaldehyde (3.56 g). The mixture was heated in an oil bath (130°) for 90 minutes, then cooled, and water (440 mL) was added. The mixture was extracted 3 times with n-hexane (150 mL). The combined organic phases were washed successively with water, 1N HCl, water, saturated NaHCO3 solution and brine. The organic solution was dried (MgSO4) and evaporated to give the title compound as colorless oil (26 g, 85 % yield). 1H NMR: 300MHz spectrum consistent with proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05414018
Quelldatensatzuspto-grants-1995_05
ORD IDord-0924ded253b34cb1b6e3517fb0eb3cab
Quellennotizuspto-grants-1995_05