HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 339508Erstellt: 25. Oktober 2026
4-Nitrobenzaldehyde → 4-(2,2,2-Trifluoroethoxy)benzaldehyde
https://huagongshe.com/reaction/339508
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Nitrobenzaldehyde | HCID 541 | — |
| Edukt | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Sodium chloride; water | HCID 57417360 | — |
| Produkt | 4-(2,2,2-Trifluoroethoxy)benzaldehyde | HCID 4770946 | 43,4% |
Reaktionsschritte
To a stirred suspension of sodium hydride (60% dispersion in mineral oil, 0.87 g, 21.8 mmol) in DMSO (20 ml) was added trifluoroethanol (3.97 g, 39.7 mmol) at 10-15° C. under an atmosphere of argon. The reaction mixture was stirred at this temperature for 20 min then 4-nitrobenzaldehyde (3.0 g, 19.85 mmol) was added in one portion. The reaction mixture was stirred at 10-15° C. for 3 h then at room temperature for 60 h. Brine (100 ml) was added cautiously to the reaction mixture followed by extraction with Et2O (3×70 ml). The combined organic extracts were washed with water, dried (MgSO4) and the solvent removed under reduced pressure to give an oil which was purified by flash chromatography (3:1 Hexane/EtOAc) to give a yellow oil which solidified on standing at room temperature to give the title compound (1.76 g, 43%) as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08895313B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-8188ad2868bb4596b140c3e2cc042c02 |
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| Quellennotiz | uspto-grants-2014_11 |
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