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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 735901생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/735901

반응식

참여 물질

역할이름HCID투입량
반응물4-Formylbenzoic acidHCID 12088—
반응물DiisopropylcarbodiimideHCID 12734—
반응물N'-hydroxydodecanimidamideHCID 178443266—
용매DichloromethaneHCID 6344—
생성물4-(3-Undecyl-1,2,4-oxadiazol-5-yl)benzaldehydeHCID 8659853155%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07592477B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-669358d4b6aa4be4a4ab0208ead4f9fd
출처 메모uspto-grants-2009_09