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HRID 39207作成日:2026年10月23日

Potassium Carbonate → Pentyl 4-(3,4-dicyanophenoxy)benzoate

https://huagongshe.com/ja/reaction/39207

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Pentyl 4-hydroxybenzoateHCID 23019—
反応物1,2-Benzenedicarbonitrile, 4-nitro-HCID 97443—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物Pentyl 4-(3,4-dicyanophenoxy)benzoateHCID 6898126285%

反応条件

温度85 °C

反応手順

A mixture of 4-nitrophthalonitrile (1.00 g, 7 mmol), pentyl 4-hydroxybenzoate (1.45 g, 7 mmol) and dried potassium carbonate (6.38 g, 46.2 mmol) in anhydrous DMF (50 mL) was stirred overnight at 85° C. under argon. After cooling to room temperature, the mixture was diluted with ethyl acetate (60 mL) and water (40 mL). The organic layer was separated, and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with a saturated solution of NaHCO3 (40 mL), brine (40 mL) and dried over anhydrous sodium sulfate. The solvents were removed in vacuo, and the crude product was purified by column chromatography on silica gel using a dichloromethane/acetonitrile mixture (20:1) as an eluent to give the product in 85% yield. [1H NMR (δ, ppm, CDCl3): 8.15 (d, 2H, J=8.7 Hz), 7.77 (d, 1H, J=8.7 Hz), 7.35 (d, 1H, J=2.3 Hz), 7.30 (d, 1H, J=8.7 Hz), 7.12 (d, 2H, J=8.7 Hz), 4.34 (2H, t, OCH2, J=6.7 Hz), 1.79 (m, 2H, CH2), 1.42 (m, 4H, CH2CH2), 0.94 (t, 3H, J=7 Hz, CH3).]

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524891B2
出典データセットuspto-grants-2013_09
ORD IDord-55bb5dca550f4cd6ac687da0cbf92ba2
出典メモuspto-grants-2013_09