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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 542751Erstellt: 27. Oktober 2026

Ammonia → N-tert-Butyl-3-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/542751

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktSulfuric AcidHCID 1118—
EduktTolueneHCID 1140—
Edukt3-Methylpyridine-2-carbonitrileHCID 819928—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
ProduktN-tert-Butyl-3-methylpyridine-2-carboxamideHCID 5463796—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

2-cyano-3-methyl pyridine (400 g) is suspended in t-BuOH (800 mL) and the mixture heated to 70° C. Concentrated sulphuric acid (400 mL) is added dropwise over 45 minutes. The reaction is complete after a further 30 minutes at 75° C. The mixture is then diluted with water (400 mL), charged with toluene (600 mL) and brought to pH 10 with concentrated aqueous ammonia. The temperature is kept at 50°-55° C. during the work up. The toluene phase is separated, the aqueous layer reextracted and the combined toluene phases are washed with water. Removal of the toluene yields an oil, N-(1,1-dimethylethyl)-3-methyl-2-pyridine carboxamide, from which solid product may crystallize. Product yield of 97% is determined by internal standard assay on gas chromatograph.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04659716
Quelldatensatzuspto-grants-1987_04
ORD IDord-becfb2b95d864db7b15047cc42b826f9
Quellennotizuspto-grants-1987_04