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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1447816생성일: 2026년 10월 27일

Hydrochloric Acid → N,2,6-Trimethylaniline hydrochloride

https://huagongshe.com/reaction/1447816

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물N-(2,6-Dimethylphenyl)formamideHCID 345859—
용매TetrahydrofuranHCID 8028—
생성물N,2,6-Trimethylaniline hydrochlorideHCID 17352627—

반응 단계

A suspension of 125.6 g. of 2,6-dimethylformanilide in 1100 ml. of dry tetrahydrofuran is cooled to 0° C. in ice-methanol. To this with constant stirring is added dropwise over a period of 3 hours 1125 ml. of 0.96 M BH3 in tetrahydrofuran. This is then allowed to warm gradually to room temperature and then heated slowly to reflux. Refluxing is maintained for 6 hours and then stirred at room temperature another 15 hours. The reaction mixture is then cooled in ice and acidified with 425 ml. of 6 N HCl. A white solid forms. The mixture is evaporated in vacuo and the water-solid slurry dissolved into 2 l. of water. The solution is made strongly alkaline (with cooling) with 50% NaOH and then extracted twice with ether (2 l.) The ether is then washed three times with 100 ml. portions of water and twice with 100 ml. portions of saturation sodium chloride solution. The ether is then dried over sodium sulfate, filtered, acidified with ethereal HCl while cooling. The white solid which forms is filtered, washed with ether and sucked dry. This is recrystallized from isopropanol methanol to give N,2,6-trimethylaniline hydrochloride (m.p. 255-257 dec.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04178387
출처 데이터셋uspto-grants-1979_12
ORD IDord-07ec9d8e201440aaae28c9ae8cf3fffc
출처 메모uspto-grants-1979_12