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HRID 2133作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/2133

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Sulfuric AcidHCID 1118—
反応物TolueneHCID 1140—
反応物3-Methylpyridine-2-carbonitrileHCID 819928—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
生成物N-tert-Butyl-3-methylpyridine-2-carboxamideHCID 546379697%

反応条件

温度70 °C

反応手順

Suspend 2-cyano-3-methyl pyridine (400 g) in t-butanol (800 mL) and heat to 70° C. Add concentrated H2SO4 (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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728703
出典データセットuspto-grants-1998_03
ORD IDord-07e514fe010d477b830fbb79e7963a40
出典メモuspto-grants-1998_03