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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21412생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/21412

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 546379697%

반응 조건

온도70 °C

반응 단계

Suspend 2-cyano-3-methyl pyridine (400 g) in t-butanol (800 mL) and heat to 70° C. Add concentrated sulphuric acid (400 mL) dropwise over 45 minutes. Maintain the temperature at 75° C., until the reaction is complete, and for an additional 30 minutes. Dilute the mixture with water (400 mL), charge with toluene (600 mL) and bring to pH 10 with concentrated aqueous ammonia. Maintain the temperature at 50°-55° C. during the work up. Separate the toluene phase, and reextract the aqueous layer. Combine toluene phases and wash with water. Remove the toluene to yield the title compound N-(1,1-dimethylethyl)-3-methyl-2-pyridine carboxamide, as an oil, from which solid product is crystallized. (Yield 97%, as determined by an internal standard assay with gas chromatography).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05422351
출처 데이터셋uspto-grants-1995_06
ORD IDord-97f4665705e544efbed0da4605e8a7f7
출처 메모uspto-grants-1995_06