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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 485284Erstellt: 24. Oktober 2026

Pyridine → 2-Nitrobenzeneacetaldehyde

https://huagongshe.com/de/reaction/485284

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktTrifluoroacetic acidHCID 6422—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt2-Nitrophenethyl alcoholHCID 27054—
EduktOxalic acid dihydrateHCID 61373—
LösungsmittelBenzeneHCID 241—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelBenzene ethyl acetateHCID 21583983—
Produkt2-NitrobenzeneacetaldehydeHCID 1084476481%

Reaktionsschritte

Trifluoroacetic acid (1.31 ml, 17 mmols) and 2.7 ml (33.3 mmols) of pyridine were added to a mixture of 5.51 g (33.3 mmols) of 2-(2-nitrophenyl)ethanol, 50 ml of dimethyl sulfoxide, 50 ml of benzene and 21 g (0.1 mol) of DCC. After stirring the mixture at room temperature for 4 hours, 300 ml of aqueous solution of 8.82 g (70 mmols) of oxalic acid dihydrate was added thereto. The resulting mixture was stirred at room temperature for 30 minutes and diluted with 500 ml of ethyl acetate. The organic layer was separated off, washed with saturated NaCl, dried over Na2SO4 and concentrated to obtain a yellow oil. The oil was subjected to silica gel column chromatography (95:5 benzene-ethyl acetate) to obtain 2-nitrophenylacetoaldehyde in the form of an unstable oil in an amount of 4.50 g (yield 81%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04536391
Quelldatensatzuspto-grants-1985_08
ORD IDord-d91480da54914daba6ee0526fbba308a
Quellennotizuspto-grants-1985_08