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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1389510생성일: 2026년 10월 27일

Hydrochloric Acid → 3-Chloro-2-methylbenzonitrile

https://huagongshe.com/reaction/1389510

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물3-Chloro-2-methylanilineHCID 6894—
반응물Sodium CyanideHCID 8929—
반응물Sodium CarbonateHCID 10340—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물3-Chloro-2-methylbenzonitrileHCID 52150852.8%

반응 조건

온도0 °C

반응 단계

Sodium cyanide (58 g, 1.18 mol) in 90 ml of water is added to cuprous chloride (44 g, 0.44 mol) in 180 ml of water while stirring mechanically in a 5 l. 3-necked flask. Evolution of heat results and the cuprous chloride dissolves. This is then cooled in an ice bath to 0° C. A milky suspension of cuprous cyanide results. To this is added 90 ml of toluene. 6 N Hydrochloric acid (125 ml) is added slowly to 3-chloro-2-methylaniline (50 g, 0.35 mol) in a 2 l. erlenmeyer flask, while cooling and swirling. A solution of sodium nitrite (25 g, 0.36 mol) in 70 ml of water is added dropwise to the hydrochloride suspension. Ice is added when required, keeping the temperature at 0° C. Anhydrous sodium carbonate is added until the diazonium hydrochloride solution is neutral to pH paper. This is then added slowly to the cold stirring cuprous cyanide suspension, the temperature not being allowed to rise above 5° C. The reaction is then stirred at 0°-5° C. for 0.5 hr, allowed to reach room temperature over a 2 hr period and then heated to 50° C. on the steam bath. After remaining at room temperature overnight, the product is steam distilled off. The distillate is extracted with benzene, washed with 10% hydrochloric acid, dried and evaporated to afford 28 g of the title compound that solidified on standing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04244966
출처 데이터셋uspto-grants-1981_01
ORD IDord-f7c8e8662b8d49d6a03703ea1fab96e2
출처 메모uspto-grants-1981_01