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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275042생성일: 2026년 10월 26일

Hydrochloric Acid → HCID 178425411, 화합물

https://huagongshe.com/reaction/275042

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물Acetic AnhydrideHCID 7918—
반응물ChlorineHCID 24526—
반응물2,6-Dichloro-3-methylanilineHCID 116529—
반응물HCID 178509066HCID 178509066—
용매Acetic AcidHCID 176—
생성물HCID 178425411HCID 178425411—

반응 조건

온도12 °C

반응 단계

A mixture of 11.6 g (0.10 mole) of 5-amino-3-mercapto-1,2,4-triazole, 12.75 g (0.0125 moles) of acetic anhydride and 100 ml of acetic acid was prepared and heated at reflux with stirring for 12 hours. Another 50 ml of acetic acid and 10 ml of water were then added and the mixture was cooled to 12° C. Chlorine (21 g, 0.3 mole) was then added to the mixture with stirring over a 15 min. period at 12°-20° C. A yellow solution was obtained. About 100 ml of volatiles were removed by distillation at 50° C. under reduced pressure. The resulting residue was combined with 2,6-dichloro-3-methylaniline (14.1 g, 0.080 mole) and the mixture heated at 115° C. for 4 hours with stirring. Concentrated aqueous hydrochloric acid (50 ml) was then added and the mixture was heated at reflux with stirring for another 5 hours. It was then allowed to cool to ambient temperature and the solids present were collected by filtration. The collected solids were placed in 200 ml of 10 percent aqueous sodium hydroxide. The insoluble material was removed by filtration and the pH of the filtrate was adjusted to 4.5 with hydrochloric acid to reprecipitate the title compound. The solids were recovered by filtration, washed with water, and dried under reduced pressure to obtain 10.1 g (28.9 percent of theory) of the title compound assaying 95 percent by high pressure liquid chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05391759
출처 데이터셋uspto-grants-1995_02
ORD IDord-1a35c5ae88114c1da25b6c61355db467
출처 메모uspto-grants-1995_02