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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1025822Erstellt: 24. Oktober 2026

Borane;tetrahydrofuran → 1-Cyclopropyl-1,2,3,4-tetrahydroquinoxaline

https://huagongshe.com/de/reaction/1025822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBorane;tetrahydrofuranHCID 2723981—
Edukt1-Cyclopropyl-1,4-dihydroquinoxaline-2,3-dioneHCID 21279695—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Cyclopropyl-1,2,3,4-tetrahydroquinoxalineHCID 6732075549%

Reaktionsschritte

To a stirred suspension of 1-cyclopropyl-1,4-dihydro-quinoxaline-2,3-dione (10.0 g, 49.45 mmol, 1.0 equiv) in tetrahydrofuran (500 mL) was added dropwise a 1 M solution of borane-tetrahydrofuran complex (108.8 mL, 108.8 mmol, 2.2 equiv; [CAS RN 14044-65-6]) and the reaction mixture stirred at room temperature over night. The solvent was removed by evaporation under reduced pressure and the crude reaction mixture extracted from a saturated aqueous solution of sodium bicarbonate (100 mL) with ethyl acetate (three times 100 mL). The combined organic phases were dried over sodium sulfate and purified by silica gel column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:ethyl acetate to give 4.2 g (49%) of the title compound as a light yellow solid. MS (ISP): m/z=175.4 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08729091B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-b0474f9d64ee40d68ed2fcead35349dd
Quellennotizuspto-grants-2014_05