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HRID 2247845作成日:2026年10月27日

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

https://huagongshe.com/reaction/2247845

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物1,4-NaphthalenediolHCID 11305—
反応物Potassium HydroxideHCID 14797—
反応物Sodium DithioniteHCID 24489—
溶媒AcetoneHCID 180—
生成物4-(Benzyloxy)naphthalen-1-olHCID 562937—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05037828
出典データセットuspto-grants-1991_08
ORD IDord-3dbb469d4090486a9073712ff1576cff
出典メモuspto-grants-1991_08