Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 506488생성일: 2026년 10월 25일
Ammonium Chloride → Ethyl 4-chloro-3-hydroxy-5-phenyl-2-(4-fluoro-2-trifluoromethylbenzoylamino)pent-4-enoate
https://huagongshe.com/reaction/506488
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | 2-Chlorocinnamaldehyde | HCID 3014042 | — |
| 반응물 | Ethyl (4-fluoro-2-trifluoromethylbenzoylamino)acetate | HCID 59432157 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethyl 4-chloro-3-hydroxy-5-phenyl-2-(4-fluoro-2-trifluoromethylbenzoylamino)pent-4-enoate | HCID 72297221 | — |
반응 단계
At −75° C., 5.0 g (0.0170 mol) of ethyl (4-fluoro-2-trifluoromethylbenzoylamino)acetate dissolved in THF were added dropwise to 25.0 ml (0.050 mol) of a 2M solution of lithium diisopropylamide in THF. After 1 h at −75° C., 3.50 g (0.021 mol) of 2-chlorocinnamaldehyde dissolved in THF were added dropwise, and the mixture was stirred at −75° C. for 1 h. Saturated NH4Cl solution was added dropwise and the mixture was warmed to RT and extracted with CH2Cl2. The combined organic phases were washed and dried, and the solvent was removed. The residue was purified chromatographically (SiO2, cyclohexane/ethyl acetate). This gave 7.5 g (96% of theory) of the title compound as a colorless solid (diastereomer mixture) which was reacted further without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07786046B2 |
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| 출처 데이터셋 | uspto-grants-2010_08 |
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| ORD ID | ord-c28b6902540445b687345a44a4ead64e |
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| 출처 메모 | uspto-grants-2010_08 |
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