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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45583Erstellt: 24. Oktober 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → 5-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-indole

https://huagongshe.com/de/reaction/45583

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
Edukt5-FluoroindolineHCID 2774463—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktSodium bicarbonate waterHCID 86585896—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-fluoro-1-(piperidin-4-yl)-2,3-dihydro-1H-indoleHCID 67417842—

Reaktionsschritte

To a solution of 5-fluoroindoline (1.0 g, 7.30 mmol) and N-Boc-4-piperidone (1.60 g, 7.50 mmol) in tetrahydrofuran (10.0 mL) was added sodium triacetoxyborohydride (1.80 g, 7.50 mmol). After stirring for 3 hours at room temperature, to the mixture were added saturated sodium bicarbonate water and ethyl acetate, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified with silica gel column (chloroform/methanol=98/2 to 90/10) to give a Boc derivative of the title compound. MS (ESI+) 321 (M++1, 100%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541585B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-e200522c45314eee9bac792acc4c12d9
Quellennotizuspto-grants-2013_09