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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1666334Erstellt: 26. Oktober 2026

Pyridine → Phenyl 6-methoxypyridin-3-ylcarbamate

https://huagongshe.com/reaction/1666334

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktTetrahydrofuranHCID 8028—
EduktPhenyl chloroformateHCID 15891—
Edukt5-Methoxypyridin-3-ylamineHCID 12703595—
ProduktPhenyl 6-methoxypyridin-3-ylcarbamateHCID 2018596296%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3-Amino-5-methoxy-pyridine (5.00 g, 40.3 mmol) was dissolved in THF (80 mL), cooled to 0° C., treated with pyridine (4.07 mL, 50.4 mmol) followed by phenylchloroformate (5.32 mL, 42.3 mmol). The reaction mixture was slowly warmed to RT over several hours and stirred an additional 12 h. The mixture was partitioned between water and EtOAc. The organic layer was separated and the aqueous layer was extracted again. The combined organic extracts were dried over sodium sulfate, filtered and concentrated to give the product as a reddish solid (9.45 g, 96%), which was used without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08044052B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-bf15aa18ac8640bd9f5cd0e1d19e0ffa
Quellennotizuspto-grants-2011_10