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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4124생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/4124

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
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 mole) of 2-(4-chlorophenoxy-methyl)-2-tert.-butyl-oxirane and 24.15 g (0.35 mole) of 1,2,4-triazole were heated under reflux in 120 ml of ethanol for 48 hours. The mixture was then concentrated, the residue was taken up in 200 ml of ethyl acetate and the ethyl acetate mixture was heated. It was then cooled in an ice bath and the solid was filtered off and rinsed with ethyl acetate. The filtrate was concentrated, the residue was dissolved in ether/hexane and the solution was gassed with hydrogen chloride. The precipitate was filtered off and rinsed with ether and the free base was obtained by adding 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-1yl)butan-2-ol of melting point 84°-87° C. were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723984
출처 데이터셋uspto-grants-1988_02
ORD IDord-d3aa4ef6e7854887855a44c964e29706
출처 메모uspto-grants-1988_02