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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 479812Erstellt: 25. Oktober 2026

Ethylene Glycol → Methyl 1,4-dioxa-8-azaspiro[4.5]decane-6-carboxylate

https://huagongshe.com/reaction/479812

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
Eduktp-Toluenesulfonic acidHCID 6101—
EduktMethyl 4-oxopiperidine-3-carboxylate hydrochlorideHCID 2724028—
LösungsmittelBenzeneHCID 241—
ProduktAmmoniaHCID 222—
ProduktMethyl 1,4-dioxa-8-azaspiro[4.5]decane-6-carboxylateHCID 20598088127,7%

Reaktionsschritte

PTSA (24.7, 130 mmol) and ethylene glycol (24.8 mL, 439 mmol) were added to methyl-4-oxo-3-piperidine carboxylate hydrochloride (90) (25.1 g, 130 mmol) in benzene (52 mL, 2.5 M). The solution was stirred and heated to reflux overnight. H2O was removed using a Dean Stark trap. When the reaction was judged complete by TLC, 5% aqueous NaHCO3 and CH2Cl2 were added, and the organic layer was removed. The aqueous layer was extracted with CH2Cl2 (5×), and the combined organics were dried over sodium sulfate, filtered and concentrated in vacuo, and purified by silica gel chromatography with 20:1 CH2Cl2:2N NH3 in EtOH to provide 91 (16.7 g, 64%). 1H NMR (CDCl3) 3.82-3.70 (4H, m), 3.48 (3H, s), 3.00-2.50 (4H, m), 2.43 (1H, t), 1.76 (1H, m), 1.30 (1H, m) ppm. 13C NMR (CDCl3): 171.83, 106.57, 64.34, 64.17, 51.36, 48.91, 46.54, 43.69, 33.97 ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06645980B1
Quelldatensatzuspto-grants-2003_11
ORD IDord-44c260cdf40c453f926b2bb096247334
Quellennotizuspto-grants-2003_11