HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76995Erstellt: 23. Oktober 2026
Potassium Iodide → (2-Acetyl-phenylamino)-phenyl-acetic acid ethyl ester
https://huagongshe.com/de/reaction/76995
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | 2'-Aminoacetophenone | HCID 11086 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Ethyl bromophenylacetate | HCID 97780 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | (2-Acetyl-phenylamino)-phenyl-acetic acid ethyl ester | HCID 59401176 | 100,3% |
Reaktionsschritte
1-(2-Aminophenyl)ethanone (250 mg, 1.85 mmol), ethyl 2-bromo-2-phenylacetate (0.22 ml, 1.23 mmol), DIPEA (0.32 mL, 1.85 mmol) and a catalytic amount of potassium iodide are dissolved in acetonitrile (4 mL) and heated under MW irradiation at 100° C. for 2 hours and then at 120° C. for 1 hour. Acetonitrile is evaporated and the crude is purified by flash chromatography (petroleum ether/EtOAc=93/7) to obtain intermediate I110 as a yellow oil (367 mg, quantitative yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835682B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-5b91be84d1ed4518a37485df7db91f75 |
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| Quellennotiz | uspto-grants-2014_09 |
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