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HRID 913717作成日:2026年10月26日

Water → 3-[(tetrahydro-2H-pyran-2-yloxy)methyl]-5-[3,5-bis(trifluoromethyl)phenyl]isoxazole

https://huagongshe.com/reaction/913717

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Phenyl isocyanateHCID 7672—
反応物1-Ethynyl-3,5-bis(trifluoromethyl)benzeneHCID 1512607—
反応物2-(2-Nitroethoxy)tetrahydropyranHCID 3748656—
溶媒AcetonitrileHCID 6342—
生成物3-[(tetrahydro-2H-pyran-2-yloxy)methyl]-5-[3,5-bis(trifluoromethyl)phenyl]isoxazoleHCID 5780042941%

反応条件

温度50 °C

反応手順

To a solution of 2-[(2-nitroethyl)oxy]tetrahydro-2H-pyran (483 μL, 3.15 mmol) and 1-ethynyl-3,5-bis(trifluoromethyl)benzene (3.0 g, 12.6 mmol) in dry acetonitrile (15 mL) were added TEA (4.4 ml, 31.5 mmol) and isocyanatobenzene (3.4 mL, 31.5 mmol) at rt. The reaction is stirred at 50° C. for 5 h. Water was added and the mixture was extracted with Et2O three times. The combined organic layers were then washed with brine once, dried over MgSO4 and concentrated in vacuo. The residue was purified by radial chromatography (0-40% EtOAc-hexanes gradient) to afford the title compound (0.51 g, 41% yield): MS (ES) m/z 418 (M+Na+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08026262B2
出典データセットuspto-grants-2011_09
ORD IDord-0bdb63be9cc6459fafce5c6cd285e8e6
出典メモuspto-grants-2011_09