Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325594생성일: 2026년 10월 27일
1-Chloro-4-(trifluoromethyl)benzene → 2-(2-Fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate
https://huagongshe.com/reaction/325594
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Chloro-4-(trifluoromethyl)benzene | HCID 7394 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-(2-Fluorobenzyloxy)ethyl-2-(4-hydroxyphenoxy)propionate | HCID 13278922 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(2-Fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate | HCID 13132188 | — |
반응 단계
33.4 g of 2-(2-fluorobenzyloxy)ethyl-2-(4-hydroxyphenoxy)propionate was dissolved in 120 ml of dimethylformamide, 15.2 g of potassium carbonate were added thereto, then the mixture was heated at 95° C. for one hour with stirring. 27.1 g of 4-trifluoromethyl chlorobenzene were added to the solution which was then heated to 95° to 100° C. for five hours. After cooling the reaction solution to room temperature, it was poured into ice-water, then extracted with toluene. The toluene layer was washed successively with 1% strength by weight sodium hydroxide solution and water, and was dried and filtered. The toluene was distilled off under reduced pressure, and further volatile by-products were removed at 100° C./0.1 mmHg. The end product of 2-(2-fluorobenzyloxy)ethyl-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionate was obtained in a yield of 20.7 g. (nD20 1.5235)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04441913 |
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| 출처 데이터셋 | uspto-grants-1984_04 |
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| ORD ID | ord-917c4f4b5fc74a62becab5a37151707f |
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| 출처 메모 | uspto-grants-1984_04 |
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