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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257738Erstellt: 26. Oktober 2026

Diethyl Ether → Methyl 5-(4-piperidyl)pentanoate

https://huagongshe.com/reaction/257738

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktDiazomethaneHCID 9550—
EduktThionyl ChlorideHCID 24386—
Edukt4-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)butanoic acidHCID 10400987—
KatalysatorPyridineHCID 1049—
KatalysatorSilver benzoateHCID 164649—
LösungsmittelMethanolHCID 887—
LösungsmittelTriethylamineHCID 8471—
ProduktMethyl 5-(4-piperidyl)pentanoateHCID 19781432—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of carboxylic acid 14 (600 mg, 2.2 mmol), ether (4.0 mL), and pyridine (2 drops) at ambient temperature was added thionyl chloride in one portion to effect an exotherm. After 25 minutes the ether, pyridine, and thionyl chloride were evaporated. The intermediate acid chloride was dissolved in ether (5 mL), cooled to 0° C., then treated with an ethereal solution of diazomethane (15 mL, ~10 mmol). After 2.0 hours the excess diazomethane was removed by purging with argon. Evaporation in situ gave a solid that was dissolved in CH3OH (10 mL) then treated sequentially with NEt3 (0.5 mL) and silver benzoate (20 mg). After 15 minutes the black reaction mixture was concentrated and the residue subjected to flash chromatography (silica, 10% ethyl acetate/hexanes) to give 15 (300 mg) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05264420
Quelldatensatzuspto-grants-1993_11
ORD IDord-30a5365b4045493d9954ed939f26fbab
Quellennotizuspto-grants-1993_11