HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 217262Erstellt: 24. Oktober 2026
Triethyl phosphite → Diethyl (2,4-dimethylphenyl)phosphonate
https://huagongshe.com/de/reaction/217262
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethyl phosphite | HCID 31215 | — |
| Edukt | 4-Iodo-m-xylene | HCID 77885 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Diethyl (2,4-dimethylphenyl)phosphonate | HCID 13836144 | 84% |
Reaktionsschritte
4-Iodo-m-xylene (4.31 mmol), triethyl phosphite (6.03 mmol) and palladium acetate (0.43 mmol) were mixed together in acetonitrile (10 ml), in a microwave tube. The vessel was sealed and placed in a microwave to react at 160° C., for 45 minutes. After cooling to room temperature, acetonitrile was removed. The crude material was purified by silica gel chromatography (eluent: stepwise gradient of ethyl acetate (0-30%) in petroleum ether) to yield Intermediate I.1 as an oil (84%). Intermediate 1.1 was characterized by the following spectroscopic data: 1H NMR (CDCl3, 400 MHz) δ (ppm) 1.32 (t, J=8.0 Hz, 6H), 2.35 (s, 3H), 2.53 (s, 3H), 4.07-4.14 (m, 4H), 7.07-7.08 (m, 2H), 7.77-7.83 (m, 1H); 31P NMR (CDCl3, 162 MHz) δ (ppm) 20.15 (s, 1P); and MS (ESI, EI+) m/z=243 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08193372B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-8c51cdd718db47179a141401467a3d1f |
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| Quellennotiz | uspto-grants-2012_06 |
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