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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542751생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/542751

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Sulfuric AcidHCID 1118—
반응물TolueneHCID 1140—
반응물3-Methylpyridine-2-carbonitrileHCID 819928—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
생성물N-tert-Butyl-3-methylpyridine-2-carboxamideHCID 5463796—

반응 조건

온도70 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04659716
출처 데이터셋uspto-grants-1987_04
ORD IDord-becfb2b95d864db7b15047cc42b826f9
출처 메모uspto-grants-1987_04