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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235059생성일: 2026년 10월 26일

Hydrochloric Acid → 4-Chloro-3-cyanobenzoic acid

https://huagongshe.com/reaction/235059

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CyanideHCID 9032—
반응물3-Amino-4-chlorobenzoic acidHCID 76092—
반응물Sodium NitriteHCID 23668193—
반응물HCID 178418546HCID 178418546—
용매WaterHCID 962—
생성물4-Chloro-3-cyanobenzoic acidHCID 2264461280.3%

반응 조건

온도5 °C

반응 단계

3-Amino-4-chlorobenzoic acid (18.72 g, 109.1 mmol), commercially available, was added to a mixture of water (200 mL) and 37% HCl (35 mL), and the resulting slurry was cooled to 5° C. A solution of NaNO2 (8.65 g, 125 mmol) in water (70 mL) was added dropwise, and the solution stirred at 5° C for 30 min. The solution was then added to a slurry consisting of water (400 mL), CuCN (9.85 g, 109 mmol),and KCN(12.06g, 185 mmol), while maintaining the temperature at5°-10° C. The mixture was stirred at 10° C. for another 30 min, and then heated to 80° C. for 1 hour. The reaction was cooled, and the pH adjusted to ~1 by addition of concentrated HCl. The solution was extracted with 5× CHCl3, and the combined extracts were rinsed with 1M HCl and brine, and dried over MgSO4. The solvent was removed in vacuo, and the crude product was recrystallized from CHCl3 /EtOAc to yield 15.9 g (80%) of the title compound. m.p. 180° C. 1H NMR (300 MHz, CDCl3) δ 10.55 (br s, 1H), 8.42 (d, 1H), 8.26 (dd, 1H), 7.68 (d, 1H). MS (DCI/NH3) m/e 213 (M+NH4)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05597823
출처 데이터셋uspto-grants-1997_01
ORD IDord-32e5b58f88124207b7781d3d6a953b4a
출처 메모uspto-grants-1997_01