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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1614723생성일: 2026년 10월 26일

Benzyl Bromide → 4-(Benzyloxy)-1,2-benzenediol

https://huagongshe.com/reaction/1614723

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Triethyl borateHCID 9009—
반응물1,2,4-BenzenetriolHCID 10787—
반응물Sodium hydrideHCID 24758—
용매DimethylformamideHCID 6228—
생성물4-(Benzyloxy)-1,2-benzenediolHCID 1550697158%

반응 단계

1.37 g of 1,2,4-trihydroxy benzene and 30 ml of anhydrous dimethylformamide were mixed together under an inert gas atmosphere and then 0.984 g of sodium hydride in suspension at 53% in oil was added at 15°-20° C. The mixture was stirred for one hour and 1.906 ml of triethyl borate were added. The mixture was stirred for one hour, and 1.29 ml of benzyl bromide in solution in 20 ml of dimethylformamide were added over 2 hours. The mixture was stirred for 16 hours at ambient temperature and then was poured into a water-ice-N hydrochloric acid mixture. Extraction took place with ethyl acetate followed by evaporation to dryness. The residue was washed with petroleum ether, and chromatographed on silica eluting with a cyclohexane-ethyl acetate (6-4) mixture to obtain 1.36 g of the crystallized expected product (Yield: 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05198571
출처 데이터셋uspto-grants-1993_03
ORD IDord-9fd5685655574b3aaa8630db1cb685b6
출처 메모uspto-grants-1993_03