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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602164Erstellt: 24. Oktober 2026

Phthalimide → N-[[1-[2-(Methoxycarbonyl)phenyl]piperidin-3-yl]methyl]phthalimide

https://huagongshe.com/de/reaction/602164

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalimideHCID 6809—
EduktTriphenylphosphineHCID 11776—
EduktMethyl 2-[3-(hydroxymethyl)piperidin-1-yl]benzoateHCID 58992598—
EduktDiethylazodicarboxylate tolueneHCID 66777355—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-[[1-[2-(Methoxycarbonyl)phenyl]piperidin-3-yl]methyl]phthalimideHCID 5899269195%

Reaktionsschritte

Triphenylphosphine (1.68 g, 6.20 mmol) and phthalimide (799 mg, 5.43 mmol) were added to methyl 2-[3-(hydroxymethyl)piperidin-1-yl]benzoate (1.29 g, 5.17 mmol) in tetrahydrofuran (10 mL). The reaction mixture was stirred at room temperature for 10 min and a 40% diethyl azodicarboxylate/toluene solution (3.52 mL, 7.76 mmol) was added. The mixture was then stirred at room temperature for 8 hours. Subsequently, water was added and the mixture was extracted with ethylacetate. The extract was washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=20:1->5:1) gave 1.85 g (95%) of the desired compound as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902367B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-0cc93c605ff844d78e7a84d99a0d7f4f
Quellennotizuspto-grants-2011_03