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HRID 735901作成日:2026年10月25日

4-Formylbenzoic acid → 4-(3-Undecyl-1,2,4-oxadiazol-5-yl)benzaldehyde

https://huagongshe.com/reaction/735901

反応式

関与物質

役割名称HCID仕込み量
反応物4-Formylbenzoic acidHCID 12088—
反応物DiisopropylcarbodiimideHCID 12734—
反応物N'-hydroxydodecanimidamideHCID 178443266—
溶媒DichloromethaneHCID 6344—
生成物4-(3-Undecyl-1,2,4-oxadiazol-5-yl)benzaldehydeHCID 8659853155%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07592477B2
出典データセットuspto-grants-2009_09
ORD IDord-669358d4b6aa4be4a4ab0208ead4f9fd
出典メモuspto-grants-2009_09