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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1367237Erstellt: 25. Oktober 2026

Diisopropylethylamine → 1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/1367237

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktBenzyl succinimido carbonateHCID 83172—
EduktMethyl 4-allylpiperidine-4-carboxylateHCID 66972977—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylateHCID 58893186—

Reaktionsschritte

A mixture of methyl 4-allylpiperidine-4-carboxylate from Step A (5.30 g, 24.2 mmol), N-(benzyloxycarbonyloxy)succinimide (7.25 g, 29.1 mmol), and N,N-diisopropylethylamine (12.7 mL, 72.7 mmol) in CH3CN (61 mL) was stirred for 16 h. The solvent was removed in vacuo and the residue was partitioned between EtOAc (100 mL) and saturated NaHCO3 (100 mL). The organic layer was separated and the aqueous layer was further extracted with EtOAc (2×100 mL). The combined organic extracts were concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 40:60, to give the title compound. MS: m/z=318 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07893079B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-84147da71ee540f2a9dd29af4f9ce166
Quellennotizuspto-grants-2011_02