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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1161492Erstellt: 25. Oktober 2026

N-Formylmorpholine → 4-Methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene-2-carbaldehyde

https://huagongshe.com/reaction/1161492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-FormylmorpholineHCID 20417—
EduktAmmonium ChlorideHCID 25517—
Edukt2-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocyclohepteneHCID 59517213—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene-2-carbaldehydeHCID 59517047—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

To a solution of 420 mg of 2-bromo-4-methoxy-8,9-dihydro-5,7-dioxa-benzocycloheptene in 10 ml of THF there was added dropwise 0.7 ml of n-butyllithium (2.66 M, hexane solution) at −70° C. under a nitrogen atmosphere. After stirring at −70° C. for 10 minutes, 0.5 ml of N-formylmorpholine was added and the temperature was raised from −70° C. to 0° C. over a period of 30 minutes. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (235 mg) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07816522B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-e0b48d1b5945417c8e033d5c1089acc4
Quellennotizuspto-grants-2010_10