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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238503Erstellt: 24. Oktober 2026

6-Nitroindoline → 1-(1-Methyl(4-piperidyl))-6-nitroindoline

https://huagongshe.com/de/reaction/238503

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-NitroindolineHCID 29757—
Edukt1-Methyl-4-piperidoneHCID 74049—
EduktSodium BicarbonateHCID 516892—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelAcetic AcidHCID 176—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt1-(1-Methyl(4-piperidyl))-6-nitroindolineHCID 18796623—

Reaktionsschritte

6-Nitroindoline (5 g) was dissolved in 200 mL of dichloroethane, N-methyl-4-piperidone (5 g) was added to the mixture, followed by 12 g NaBH(OAc)3 and 1 mL of glacial AcOH. The mixture was stirred at RT overnight. Saturated NaHCO3 solution (200 mL) was added to the reaction mixture and stirred for 1 h. The resulting mixture was separated by separation funnel, the organic layer was extracted once with saturated NaHCO3 solution and once with brine. The resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel with 2:1 EtOAc:MeOH to afford an orange oil. MS: 262 (M+1). Calc'd. for C14H19N3O2—261.32.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642624B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-7d1fd85e774f4ec59f2291df1b4171fd
Quellennotizuspto-grants-2014_02