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HRID 1506190作成日:2026年10月25日

Water → Methyl N-(4-methylpyridin-3-yl)carbamate

https://huagongshe.com/reaction/1506190

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Dimethyl CarbonateHCID 12021—
反応物3-Amino-4-picolineHCID 137935—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl N-(4-methylpyridin-3-yl)carbamateHCID 1167272588.2%

反応条件

温度17.5 °C

反応手順

Potassium tert-butoxide (10.3 g, 92.5 mmol) in tetrahydrofuran (25 mL) was stirred at 23 to 27° C. for 30 minutes, and dimethyl carbonate (4.67 mL, 55.5 mmol) was added while the temperature was kept at 35° C. or below. To the reaction mixture, 3-amino-4-methylpyridine (5.00 g, 46.2 mmol) in tetrahydrofuran (40 mL) stirred at 32 to 38° C. for 90 minutes was added dropwise at 20 to 35° C. over 2 hours with stirring. The resulting reaction mixture was cooled to 15 to 20° C., stirred with water (25 mL) at 25° C. or below for 1 hour and extracted with tetrahydrofuran. The organic layer was azeotropically distilled with toluene under reduced pressure to a volume of about 50 mL and stirred at 23 to 27° C. for one day. The precipitated solid was collected by filtration, washed with toluene and dried under reduced pressure to give the title compound as a brown solid (6.77 g, yield 88%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09216999B2
出典データセットuspto-grants-2015_12
ORD IDord-ef8142deca094bfc9a6e6550347246a7
出典メモuspto-grants-2015_12