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

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%).

1. customThe resulting reaction mixture
2. stirringwas stirred overnight at rt
3. filtrationThe reaction was filtered
4. washthe collected solid washed with DCM
5. concentrationthe solvent was concentrated in vacuo
6. temperatureThe residue was heated at 115° C. for 5 h in a mixture of toluene (285 mL) and pyridine (115 mL)
7. customThe solvents were evaporated off
8. customthe resulting residue was purified on column (SiO2, c-Hex/EtOAc 20/1)

ORDレコード

ord-669358d4b6aa4be4a4ab0208ead4f9fd

出典データセット

uspto-grants-2009_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07592477B2