Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 48057생성일: 2026년 10월 24일
Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)- → 3-(3-Phenoxyphenyl)-2-[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]-5-(trifluoromethyl)oxazolidine
https://huagongshe.com/ko/reaction/48057
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)- | HCID 118803 | — |
| 반응물 | 3-[(n-3-Phenoxy-phenyl)amino]1,1,1-trifluoro-2-propanol | HCID 23506063 | — |
| 촉매 | zinc(II)iodide | HCID 9883512 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3-(3-Phenoxyphenyl)-2-[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]-5-(trifluoromethyl)oxazolidine | HCID 10117845 | 92% |
반응 단계
A toluene solution (5 mL) of 3-(1,1,2,2-tetrafluoroethoxy)benzaldehyde (0.45 g, 2.0 mol) and N-(3-phenoxyphenyl)-3-amino-1,1,1-trifluoro-2-propanol (0.60 g, 2.0 mmol) was refluxed in the presence of molecular sieves and ZnI2 (˜5 mg) for 18 h under N2. The reaction mixture was filtered to remove the sieves, and the filtrate was diluted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and evaporated to give 0.92 g (92%) of the desired 3-(3-phenoxyphenyl)-2-[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]-5-(trifluoromethyl) oxazolidine product as a colorless oil. The formation of the desired product was monitored by the disappearance of the aldehyde peak (δ˜10) in the 1H NMR spectrum. HRMS calcd. 502.1253 [M+H]+, found: 502.1220.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06699898B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-4e719f0b4b664b1f9df11d800b931e79 |
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| 출처 메모 | uspto-grants-2004_03 |
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