Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Chlorobenzene → Ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Chlorobenzene | HCID 7964 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | p-(4-(Trifluoromethyl)phenoxy)phenol | HCID 170230 | — |
| 반응물 | Ethyl 4-bromopent-2-enoate | HCID 53952747 | — |
| 촉매 | N,N-Dibutyl-N-ethylbutan-1-aminium bromide | HCID 19043781 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate | HCID 156921 | 96% |
반응 단계
In a reactor, 100 ml of chlorobenzene and 100 ml of water were charged and then, 95.3 g (0.375 mole) of 4-(4-trifluoromethylphenoxy)phenol, 85.4 g (0.412 mole) of ethyl 4-bromo-2-pentenoate, 39.0 g (0.281 mole) of potassium carbonate and 1.1 g (0.00375 mole) of tributylethyl ammonium bromide were added. The mixture was refluxed with stirring for 6 hours to react them, and the water phase was removed and the organic phase was washed with 5% hydrochloric acid and with water and then, chlorobenzene, ethyl 4-bromo-2-pentenoate and low boiling by-products were distilled off at 100° C. under a reduced pressure of 0.02 to 0.05 mmHg to obtain 137.0 g of ethyl 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoate. The yield was 96.0%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04254262 |
| 출처 데이터셋 | uspto-grants-1981_03 |
| ORD ID | ord-8cc3e1a347fb4f15b35b9cd8dfe0e993 |
| 출처 메모 | uspto-grants-1981_03 |