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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 973676생성일: 2026년 10월 25일

Water → 2-(2,6-Dichloro-4-trifluoromethylphenylhydrazono)acetaldehyde

https://huagongshe.com/reaction/973676

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물GlyoxalHCID 7860—
반응물[2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazineHCID 688223—
용매Acetic AcidHCID 176—
생성물2-(2,6-Dichloro-4-trifluoromethylphenylhydrazono)acetaldehydeHCID 86745202—

반응 단계

A solution of 2,6-dichloro-4-trifluoromethylphenylhydrazine (5 g) in acetic acid was added dropwise to a mixture of 40% aqueous glyoxal (50 ml) and water (400 ml). The mixture was stirred at room temperature for 2 hours and solid collected by filtration. A sample was recrystallised from ethanol to give 2-(2,6-dichloro-4-trifluoromethylphenylhydrazono)acetaldehyde, m.p. 131°-133°. This crude product (2.85 g) in ethanol (30 ml) was added to a solution of hydroxylamine hydrochloride (0.7 g) in water (10 ml), which had been neutralized with sodium acetate (0.82 g). The mixture was stirred at room temperature and then extracted with ethyl acetate. The extract was washed with brine, dried and evaporated to 2-(2,6-dichloro-4-trifluoromethylphenylhydrazono)acetaldehyde oxime. This was then treated with copper sulphate, in a similar manner to Example 1, to give 2-(2,6-dichloro-4-trifluoromethylphenyl)-2H-1,2,3-triazole 1-oxide, m.p. 153°-154°, which in turn was treated with trimethyloxonium tetrafluoroborate and sodium methanethiolate, in a similar manner to Example 3, to give 2-(2,6-dichloro-4-trifluoromethylphenyl)-4-methylthio-2H-1,2,3-triazole, m p. 100°-101°. (Compound 11)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05064844
출처 데이터셋uspto-grants-1991_11
ORD IDord-c31edd0bb716474ba2a50c1673e3bdf9
출처 메모uspto-grants-1991_11