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HRID 1359272作成日:2026年10月27日

Benzyl Bromide → (3-(Benzyloxy)-6-methylpyridin-2-yl)methanol

https://huagongshe.com/reaction/1359272

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物3-Hydroxy-2-hydroxymethyl-6-methylpyridineHCID 135128—
溶媒DimethylformamideHCID 6228—
生成物(3-(Benzyloxy)-6-methylpyridin-2-yl)methanolHCID 22711808—

反応条件

温度60 °C

反応手順

100 g of 3-hydroxy-6-methyl-2-pyridine methanol and 150 g of potassium carbonate were suspended in 400 ml of N,N-dimethylformamide. Under heating under stirring 60° C. in an oil bath, 85 ml of benzyl bromide was added dropwise thereinto. Further, after heating under stirring for 30 minutes, insoluble matters were filtered off. Water was added to the filtrate, and the mixture was extracted with ethyl acetate. The organic phase was washed with water and brine, dried over anhydrous magnesium sulfate and the solvent was removed. The residue was recrystallized from ethanol/hexane, to give 145 g of the target compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06599917B1
出典データセットuspto-grants-2003_07
ORD IDord-9428576bcc0e46c2af241a37be4cb3bb
出典メモuspto-grants-2003_07