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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327646생성일: 2026년 10월 24일

Pyridine → 1,2-Propanediol, 3-((o-benzyloxy)phenoxy)-

https://huagongshe.com/ko/reaction/327646

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물GlycidolHCID 11164—
반응물2-BenzyloxyphenolHCID 80459—
용매EthanolHCID 702—
생성물1,2-Propanediol, 3-((o-benzyloxy)phenoxy)-HCID 302205273%

반응 단계

A solution of 49.6 g (0.248 mole) of 2-benzyloxyphenol, 22.2 g (0.3 mole) of glycidol, 2 ml of pyridine and 150 ml of absolute ethanol was heated at reflux overnight. The dark solution was concentrated to give an oil which gradually crystallized. The solid was purified by column chromatography on 1.2 kg of silica gel eluted with 0-25% acetone in benzene. Appropriate fractions were combined and concentrated to yield 49.5 g (73%) of the title compound as a white solid, mp 84°-85° C. (carbon tetrachloride) (lit.1 mp 81°-82.5° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05273993
출처 데이터셋uspto-grants-1993_12
ORD IDord-c8b2f1c968664e6e8f59e35c9755838e
출처 메모uspto-grants-1993_12