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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2247845생성일: 2026년 10월 27일

Benzyl Chloride → 4-(Benzyloxy)naphthalen-1-ol

https://huagongshe.com/reaction/2247845

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl ChlorideHCID 7503—
반응물1,4-NaphthalenediolHCID 11305—
반응물Potassium HydroxideHCID 14797—
반응물Sodium DithioniteHCID 24489—
용매AcetoneHCID 180—
생성물4-(Benzyloxy)naphthalen-1-olHCID 562937—

반응 단계

23.7 g. (0.147 mole) 1,4-Dihydroxynaphthalene (purified by shaking an ethereal solution thereof with sodium dithionite solution) are dissolved in 200 ml. acetone. After adding 20.3 g. (0.147 mole) of pulverised potassium hydroxide and heating to reflux temperature, 18.6 g. (16.9 ml.) benzyl chloride are added dropwise thereto in the course of 60 minutes. The reaction mixture is thereafter heated under reflux for 4 hours while stirring, evaporated and the residue is mixed with 100 ml. water and extracted with diethyl ether. The ethereal solution is dried with anhydrous magnesium sulphate, filtered and evaporated. The tar-like residue is extracted with cyclohexane. The combined extracts are cooled, considerable amounts of a tarry product thereby first separating out. Thereafter, the pure compound crystallises out. It is washed with cyclohexane and dried. Yield 4.3 g. (11.9% of theory); m.p. 118°-119° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05037828
출처 데이터셋uspto-grants-1991_08
ORD IDord-3dbb469d4090486a9073712ff1576cff
출처 메모uspto-grants-1991_08