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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1165704생성일: 2026년 10월 26일

1H-1,2,4-Triazole → alpha-((4-Chlorophenoxy)methyl)-alpha-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol

https://huagongshe.com/reaction/1165704

반응식

참여 물질

역할이름HCID투입량
반응물1H-1,2,4-TriazoleHCID 9257—
반응물2-tert-Butyl-2-[(4-chlorophenoxy)methyl]oxiraneHCID 12763621—
용매EthanolHCID 702—
생성물alpha-((4-Chlorophenoxy)methyl)-alpha-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanolHCID 12367665%

반응 단계

72.15 g (0.3 mol) of 2-(4-chlorophenoxy-methyl)-2-tert.-butyl-oxirane and 24.15 g (0.35 mol) of 1,2,4-triazole were heated under reflux in 120 ml of ethanol for 48 hours. The mixture was then concentrated, and the residue was taken up in 200 ml of ethyl acetate and the solution heated. The solution was thereafter cooled in an ice bath, and the solid material was filtered off under suction and was washed with ethyl acetate. The filtrate was concentrated and the residue was dissolved in ether/hexane, and the solution was treated with gaseous hydrogen chloride. The precipitate was filtered off under suction and washed with ether, and the free base was obtained by the addition of ethyl acetate/1N sodium hydroxide solution. 60.2 g (65% of theory) of 2-(4-chlorophenoxy-methyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol of melting point 84°-87° C. were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04911750
출처 데이터셋uspto-grants-1990_03
ORD IDord-def0e12185ea463e8c1800b44c44b3c9
출처 메모uspto-grants-1990_03