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HRID 77270作成日:2026年10月24日

Water → 3-(4-Ethoxy-2-oxocyclohex-3-enyl)propyl 2-(methylamino)benzoate

https://huagongshe.com/ja/reaction/77270

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物N-Methylisatoic anhydrideHCID 25160—
反応物3-Ethoxy-6-(3-hydroxypropyl)cyclohex-2-enoneHCID 25241751—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物3-(4-Ethoxy-2-oxocyclohex-3-enyl)propyl 2-(methylamino)benzoateHCID 2524175245%

反応条件

温度65 °C

反応手順

Alcohol 3 (180 mg, 0.89 mmol), NEt3 (0.56 mL) and catalytic DMAP were added to a solution of N-methylisatoic anhydride (220 mg, 0.89 mmol) in dry DMF (2.0 mL) at rt. After stirring overnight, the solution was warmed to 65° C. for 3 h. After cooling to rt, water was added and this mixture was extracted with ethyl acetate (5×50 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered, and evaporated to give the crude product, which was purified by flash column chromatography to afford 87.0 mg (45% yield) of 4 as a white solid: 1H NMR (300 MHz, CDCl3) δ 7.85 (1H, m), 7.33 (1H, m), 6.56 (2H, m), 5.27 (1H, s), 4.22 (2H, t, J=5.2 Hz), 3.85 (2H, q, J=7.0 Hz), 2.86 (3H, s), 2.39 (2H, t, J=5.3 Hz), 2.04-1.41 (7H, m), 1.31 (3H, t, J=7.0 Hz); 13C NMR (75 MHz, CDCl3) δ 201.1, 176.8, 168.7, 151.7, 134.7, 131.7, 115.0, 111.3, 110.6, 102.5, 101.9, 64.7, 64.5, 64.3, 44.9, 30.0, 28.2, 26.6, 26.5, 26.4, 14.3; ESI MS m/z 354 (M++Na+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841132B2
出典データセットuspto-grants-2014_09
ORD IDord-958ff28899cb4cf1895dc65cd340913b
出典メモuspto-grants-2014_09