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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 1H-1,2,4-Triazole | HCID 9257 | — |
| 반응물 | 2-tert-Butyl-2-[(4-chlorophenoxy)methyl]oxirane | HCID 12763621 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | alpha-((4-Chlorophenoxy)methyl)-alpha-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol | HCID 123676 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04723984 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-d3aa4ef6e7854887855a44c964e29706 |
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| 출처 메모 | uspto-grants-1988_02 |
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