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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2215078Erstellt: 25. Oktober 2026

Pyridine → methyl(4R)-3-(6-cyanohexyl)-2-oxo-1,3-oxazolidine-4-carboxylate

https://huagongshe.com/reaction/2215078

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktPhosgeneHCID 6371—
Eduktmethyl N-(6-cyanohexyl)-D-serinateHCID 86606385—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
Produktmethyl(4R)-3-(6-cyanohexyl)-2-oxo-1,3-oxazolidine-4-carboxylateHCID 69659745—

Reaktionsschritte

To a solution of amine 2-1 (620 mg) and pyridine (0.48 mL) in dichloromethane (10 mL) at 0° C. was added a solution of phosgene in toluene (1.72 mL, 1.9 M) and the mixture was stirred at the temperature for 1 h. The mixture was diluted with dichloromethane and washed with 1 N HCl and brine, and dried over Na2SO4. Filtration and concentration of the filtrate gave the crude product which was purified by chromatography. Eluting with 60% ethyl acetate in hexanes afforded the desired product 2-2 (560 mg). 1H NMR (400 MHz, acetone-d6): δ 4.61 (dd, 1H), 4.52 (t, 1H), 4.35 (dd, 1H), 3.80 (s, 3H), 3.48 (m, 1H), 3.15 (m, 1H), 2.47 (t, 2H), 1.75–1.35 (m, 8H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07109223B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-82ec6ef3a7c1491798f57d621906b4a4
Quellennotizuspto-grants-2006_09