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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1521생성일: 2026년 10월 23일

Methyl 5-(benzyloxy)-2-hydroxybenzoate → 4-(Benzyloxy)-2-(hydroxymethyl)phenol

https://huagongshe.com/ko/reaction/1521

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 5-(benzyloxy)-2-hydroxybenzoateHCID 13026913—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물4-(Benzyloxy)-2-(hydroxymethyl)phenolHCID 19690921—

반응 조건

온도0 °C

반응 단계

Lithium aluminium hydride (0.235 g, 6.2 mMol) was suspended in tetrahydrofuran (25 ml) and cooled to 0° C. 5-Benzyloxy-2-hydroxy benzoic acid methyl ester (2 g, 7.75 mMol) in tetrahydrofuran (10 ml) was added dropwise, via cannula. The mixture was warmed to room temperature and stirred for 20 minutes. The reaction was then cooled to 0° C. and cautiously quenched by the addition of water (0.5 ml), 2M sodium hydroxide solution (0.5 ml), and water (1 ml). The resulting mixture was stirred at room temperature for 30 minutes and filtered. The filtrate was evaporated in vacuo to yield 4-benzyloxy-2-hydroxymethyl phenol as a clear oil which was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726165
출처 데이터셋uspto-grants-1998_03
ORD IDord-d01bdcbca7ae4670b375df3584280165
출처 메모uspto-grants-1998_03