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HRID 2073965Erstellt: 25. Oktober 2026

Diethyl oxalacetate → Diethyl furo[3,2-b]pyridine-5,6-dicarboxylate

https://huagongshe.com/reaction/2073965

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl oxalacetateHCID 66951—
Edukt3-Azidofuran-2-carbaldehydeHCID 4153776—
Edukt3-Aminofuran-2-carbaldehydeHCID 12210211—
KatalysatorPiperidineHCID 8082—
LösungsmittelEthanolHCID 702—
ProduktDiethyl furo[3,2-b]pyridine-5,6-dicarboxylateHCID 1375250424%

Reaktionsschritte

3-Amino-2-formylfuran, prepared from 3-azido-2-formylfuran (8.9 g 0.065 mol) is dissolved in ethanol and to this solution diethyl oxalacetate (12.23 g, 0.065 mol) and ten drops of piperidine are added. In addition pulverized 3A° molecular sieve is added and the reaction stirred at 65°-60° C. for three hours, then additional diethyl oxalacetate (2.2 g) is added. The reaction is essentially complete after 12 hours at 55°-60° C. On cooling the reaction is filtered, and the filtrate concentrated and then dissolved in ethyl acetate, water washed, then brine washed, dried over anhydrous magnesium sulfate and stripped to dryness. The residue is dissolved in 3:1 hexane:ethyl acetate and passed through a flash chromatographic column in two stages. First it is filtered by vacuum through a four to five inch pad of silica from which the last three fractions containing the required product are collected and combined. These combined fractions are then passed through a six inch column eluting under pressure with ethyl acetate:hexane 3:1 and 2.1. Diethyl furo[3,2-b]-pyridine-5,6-dicarboxylate 4.15 g (24%) is obtained after crystallization from hexane-ether, of mp 60°64° C., and with a mas spectrum m/e of 264.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04920226
Quelldatensatzuspto-grants-1990_04
ORD IDord-7ac6b5b022b74228a3ac4d04cac4611c
Quellennotizuspto-grants-1990_04