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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39207생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Pentyl 4-hydroxybenzoateHCID 23019—
반응물1,2-Benzenedicarbonitrile, 4-nitro-HCID 97443—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Pentyl 4-(3,4-dicyanophenoxy)benzoateHCID 6898126285%

반응 조건

온도85 °C

반응 단계

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).]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524891B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-55bb5dca550f4cd6ac687da0cbf92ba2
출처 메모uspto-grants-2013_09