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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 253060Erstellt: 25. Oktober 2026

Water → Benzyl 4-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/253060

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
EduktBenzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktBenzyl 4-methoxypiperidine-1-carboxylateHCID 2302430145%

Reaktionsschritte

To a solution of 1-benzyloxycarbonyl-4-hydroxypiperidine (1.3 g) in dimethylformamide (10 mL) was added sodium hydride (360 mL) under ice cooling and the mixture was stirred at room temperature under nitrogen-gas atmosphere for 1 hours. To the reaction mixture was added methyl iodide (374 μL) under ice-cooling and the mixture was stirred at the same temperature for 1 hour and at room temperature for 2 hours. To the reaction mixture was added water and ethyl acetate and the mixture was stirred. The organic layer washed with a brine, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo and the resultant crude product was purified by column chromatography on silica gel (solvent: hexane/ethyl acetate=88/12 to 70/30) to obtain 1-benzyloxycarbonyl-4-methoxypiperidine (622 mg, yield: 45%) as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07872006B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-e9dd1c0189ef49e99991622f5a437a99
Quellennotizuspto-grants-2011_01