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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Formylbenzoic acidHCID 12088—
EduktDiisopropylcarbodiimideHCID 12734—
EduktN'-hydroxydodecanimidamideHCID 178443266—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(3-Undecyl-1,2,4-oxadiazol-5-yl)benzaldehydeHCID 8659853155%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07592477B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-669358d4b6aa4be4a4ab0208ead4f9fd
Quellennotizuspto-grants-2009_09