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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1076463생성일: 2026년 10월 26일

Potassium Hydroxide → 3-(m-Phenoxyphenoxy)-3'-(o-phenoxyphenoxy)biphenyl

https://huagongshe.com/reaction/1076463

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물2-Hydroxydiphenyl etherHCID 75491—
반응물3-Chloro-3'-(m-phenoxyphenoxy)biphenylHCID 21536922—
촉매CopperHCID 23978—
용매TolueneHCID 1140—
생성물3-(m-Phenoxyphenoxy)-3'-(o-phenoxyphenoxy)biphenylHCID 2153693061%

반응 단계

A 500 ml. reaction flask equipped with stirrer, condenser, and Dean Stark trap was charged with 191 g. (1.03 moles) of o-phenoxyphenol, 50 ml. of toluene and 39.5 g. (0.70 mole) of potassium hydroxide. The mixture was heated to reflux and water azeotroped from the system. Diglyme (100 ml.) was then added followed by 20 g. (0.053 mole) of 3-chloro-3'-(m-phenoxyphenoxy)biphenyl over a 30 minute period. To this mixture 2.5 g. of cuprous chloride and 0.5 g. of copper powder was added and after removing the diglyme be distillation, the reaction mixture was heated at 230°-240° for 18 hours. The mixture was cooled, diluted with 500 ml. of ether and centrifuged to remove copper and potassium salts. The salts were washed with additional ether, and the ether fractions combined and washed with 25% potassium hydroxide solution followed by water washing to neutrality. After drying the ethereal solution over magnesium sulfate, and removing ether in vacuo, the resulting oil was distilled to give 16.9 g of the desired product, bp 255°-260°/0.02 mm.; nD25 1.6480.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03957666
출처 데이터셋uspto-grants-1976_05
ORD IDord-95bad390f76a4b19915d1471fd4e2366
출처 메모uspto-grants-1976_05