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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1359272생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1359272

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물3-Hydroxy-2-hydroxymethyl-6-methylpyridineHCID 135128—
용매DimethylformamideHCID 6228—
생성물(3-(Benzyloxy)-6-methylpyridin-2-yl)methanolHCID 22711808—

반응 조건

온도60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06599917B1
출처 데이터셋uspto-grants-2003_07
ORD IDord-9428576bcc0e46c2af241a37be4cb3bb
출처 메모uspto-grants-2003_07