HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 735901Erstellt: 25. Oktober 2026
4-Formylbenzoic acid → 4-(3-Undecyl-1,2,4-oxadiazol-5-yl)benzaldehyde
https://huagongshe.com/reaction/735901
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Formylbenzoic acid | HCID 12088 | — |
| Edukt | Diisopropylcarbodiimide | HCID 12734 | — |
| Edukt | N'-hydroxydodecanimidamide | HCID 178443266 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-(3-Undecyl-1,2,4-oxadiazol-5-yl)benzaldehyde | HCID 86598531 | 55% |
Reaktionsschritte
To a solution of 4-carboxybenzaldehyde (20.0 g, 133.2 mmol) in anhydrous DCM (500 mL) was added DIC (18.42 g, 146.5 mmol). The mixture was stirred at rt for 30 min then a solution of N-hydroxydodecanimidamide (31.41 g, 146.5 mmol) in anhydrous DCM (500 mL) was added in one portion. The resulting reaction mixture was stirred overnight at rt. The reaction was filtered, the collected solid washed with DCM and the solvent was concentrated in vacuo. The residue was heated at 115° C. for 5 h in a mixture of toluene (285 mL) and pyridine (115 mL). The solvents were evaporated off and the resulting residue was purified on column (SiO2, c-Hex/EtOAc 20/1) to give the title compound as a white solid (24.0 g, 55%). 1H NMR (CDCl3, 300 MHz) δ 10.1 (s, 1H), 8.18 (d, 2H, J=8.3 Hz), 7.94 (d, 2H, J=8.3 Hz), 2.33 (t, 2H, J=7.4 Hz), 1.74-1.58 (m, 2H), 1.43-1.18 (m, 16H), 0.87 (m, 3H). HPLC (Condition A), Rt: 5.83 min (HPLC purity: 99.6%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07592477B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-669358d4b6aa4be4a4ab0208ead4f9fd |
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| Quellennotiz | uspto-grants-2009_09 |
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