HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 474577Erstellt: 24. Oktober 2026
Ammonium Chloride → 3-(2,4,6-Trifluoro-phenyl)-acrylic acid ethyl ester
https://huagongshe.com/de/reaction/474577
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Ethyl (dimethoxyphosphinoyl)acetate | HCID 67555 | — |
| Edukt | 2,4,6-Trifluorobenzaldehyde | HCID 521845 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Produkt | 3-(2,4,6-Trifluoro-phenyl)-acrylic acid ethyl ester | HCID 57412779 | 87% |
Reaktionsschritte
To the solution of ethyl[bis(methyloxy)phosphoryl]acetate (1.980 mL, 11.99 mmol) in THF-DMF (60 mL, v/v=5:1) at 0° C. was added t-BuOK (1.458 g, 12.99 mmol) portion wise. The resultant mixture was stirred at room temperature for 30 minutes, then mixed with a solution of 2,4,6-trifluorobenzaldehyde (1.6 g, 9.99 mmol) in THF (10 mL) at 0° C. It was allowed to warm to room temperature and the mixture was stirred for 45 min. It was mixed with aqueous ammonium chloride and then extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated. The residue was purified by a flash column chromatography to give the title compound as a pale yellow oil (2.0 g, 87% yield). LCMS: rt=3.52 min, [M+H+]=231.1
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08637536B2 |
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| Quelldatensatz | uspto-grants-2014_01 |
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| ORD ID | ord-e0957e9540054c5f81479c9091b0c6c2 |
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| Quellennotiz | uspto-grants-2014_01 |
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