참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 2-Hydroxydiphenyl ether | HCID 75491 | — |
| 반응물 | 3-Chloro-3'-(m-phenoxyphenoxy)biphenyl | HCID 21536922 | — |
| 촉매 | Copper | HCID 23978 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3-(m-Phenoxyphenoxy)-3'-(o-phenoxyphenoxy)biphenyl | HCID 21536930 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03957666 |
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| 출처 데이터셋 | uspto-grants-1976_05 |
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| ORD ID | ord-95bad390f76a4b19915d1471fd4e2366 |
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| 출처 메모 | uspto-grants-1976_05 |
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