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HRID 48057Erstellt: 23. Oktober 2026
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/de/reaction/48057
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)- | HCID 118803 | — |
| Edukt | 3-[(n-3-Phenoxy-phenyl)amino]1,1,1-trifluoro-2-propanol | HCID 23506063 | — |
| Katalysator | zinc(II)iodide | HCID 9883512 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 3-(3-Phenoxyphenyl)-2-[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]-5-(trifluoromethyl)oxazolidine | HCID 10117845 | 92% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06699898B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-4e719f0b4b664b1f9df11d800b931e79 |
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| Quellennotiz | uspto-grants-2004_03 |
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