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HRID 1524Erstellt: 26. Oktober 2026

Potassium Carbonate → (R)-5-[N-(t-Butyloxycarbonyl)-2-aminopropyl]-1,3-benzodioxole-2,2-dicarboxylic acid, diethyl ester

https://huagongshe.com/reaction/1524

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktPropanedioic acid, 2,2-dibromo-, 1,3-diethyl esterHCID 69427—
Edukt(R)-2-(3,4-Dihydroxyphenyl)propylcarbamic acid, t-butyl esterHCID 86752190—
LösungsmittelAcetoneHCID 180—
Produkt(R)-5-[N-(t-Butyloxycarbonyl)-2-aminopropyl]-1,3-benzodioxole-2,2-dicarboxylic acid, diethyl esterHCID 54476420—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A solution of (R)-2-(3,4-dihydroxyphenyl)propylcarbamic acid, t-butyl ester. (1.07 g, 4 mMol) in acetone (25 ml) containing potassium carbonate (3 equiv, 1.66 g, 12 mMol) was stirred at 60° C. under an argon atmosphere for 1 hour. After cooling to ambient temperature, a solution of diethyl dibromomalonate (1.27 g, 4 mMol) in acetone (7 ml) was added and the reaction was stirred at ambient temperature for 18 hours. The suspension was filtered and the residue was washed with ethyl acetate. The filtrates were combined, evaporated and the residue was partitioned between ethyl acetate (200 ml) and dilute hydrochloric acid (100 ml, pH5). The organic layer was separated, washed with water (2×100 ml) and brine (100 ml), dried (MgSO4) and evaporated. The residue was purified by column chromatography on silica gel eluting with 25% ethyl acetate in n-hexane giving the title compound as an oil;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726165
Quelldatensatzuspto-grants-1998_03
ORD IDord-15507b7830194c87ab4d8306a193e36d
Quellennotizuspto-grants-1998_03