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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 647977생성일: 2026년 10월 25일

Benzyl Alcohol → 1-[(6-Methylpyridin-3-yl)oxy]-3-[(propan-2-yl)amino]propan-2-ol

https://huagongshe.com/reaction/647977

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl AlcoholHCID 244—
반응물2-Methyl-5-hydroxypyridineHCID 14275—
반응물Potassium HydroxideHCID 14797—
반응물1-(Propan-2-yl)azetidin-3-olHCID 544677—
용매Diethyl EtherHCID 3283—
생성물1-[(6-Methylpyridin-3-yl)oxy]-3-[(propan-2-yl)amino]propan-2-olHCID 20483467—

반응 조건

온도150 °C

반응 단계

A mixture of 6.1 g of 6-methyl-3-pyridinol, 5.5 g of 1-isopropyl-3-azetidinol, 0.3 g of potassium hydroxide and 25 ml of benzyl alcohol is stirred for 16 hours under nitrogen in a bath at 150° C. After cooling, the reaction mixture is diluted with 50 ml of ether and extracted with 30 ml of 4 N hydrochloric acid. The aqueous phase is separated off, rendered alkaline with concentrated sodium hydroxide solution and extracted with 100 ml of methylene chloride. 3-(3'-Isopropylamino-2'-hydroxy-propoxy)-6-methyl-pyridine is isolated from the crude product thus obtained by bulb tube distillation at 130°-140° C. bath temperature and 0.04 mm Hg. It is identical in its properties with the product obtained in Example 19.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04410530
출처 데이터셋uspto-grants-1983_10
ORD IDord-648e995c10494033a116e7bda05572b5
출처 메모uspto-grants-1983_10