Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → 2-Trifluoromethyl-4-(4-ethoxyphenoxy)-1-benzyloxybenzene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-Ethoxyphenol | HCID 12150 | — |
| 반응물 | 1-(Benzyloxy)-4-bromo-2-(trifluoromethyl)benzene | HCID 18620160 | — |
| 촉매 | Copper | HCID 23978 | — |
| 생성물 | 2-Trifluoromethyl-4-(4-ethoxyphenoxy)-1-benzyloxybenzene | HCID 21466273 | 41.8% |
반응 단계
Then, 5.10 g of 4-bromo-2-trifluoromethyl-1-benzyloxybenzene, 2.34 g of p-ethoxyphenol, 2.13 g of potassium carbonate, 100 mg of copper and 200 mg of cuprous chloride were charged into a reaction vessel, and stirred at 130° C. to 140° C. for 5 hours. The reaction solution was cooled to room temperature, poured into ice-water and then acidified by adding 10% hydrochloric acid. The solution was extracted twice with 100 ml of diethyl ether. Then, the ether layers were combined, washed with water, dried over anhydrous magnesium sulfate and concentrated to give a crude product. This crude product was subjected to silica gel chromatography to give 2.50 g of 2-trifluoromethyl-4-(4-ethoxyphenoxy)-1-benzyloxybenzene (yield, 41%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05530015 |
| 출처 데이터셋 | uspto-grants-1996_06 |
| ORD ID | ord-98cf78ada01347c892953c47b824b79e |
| 출처 메모 | uspto-grants-1996_06 |