Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477200생성일: 2026년 10월 24일
1H-1,2,4-Triazole → alpha-((4-Chlorophenoxy)methyl)-alpha-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol
https://huagongshe.com/ko/reaction/477200
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1H-1,2,4-Triazole | HCID 9257 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 2-tert-Butyl-2-[(4-chlorophenoxy)methyl]oxirane | HCID 12763621 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | alpha-((4-Chlorophenoxy)methyl)-alpha-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanol | HCID 123676 | 52% |
반응 단계
A mixture of 30 g of 2-(4-chlorophenoxymethyl)-2-tert.-butyloxirane, 9.8 g of 1,2,4-triazole and 1.2 g of solid potassium hydroxide in 70 ml of toluene and 7.5 ml of dimethyl sulphoxide was heated under reflux for 6 hours. After cooling to room temperature, 2 g of silica gel were added to the reaction mixture and it was then filtered. 75 ml of semi-concentrated hydrochloric acid were added to the filtrate, and the crystals which separated out thereby were filtered off with suction. Then 80 ml of water and aqueous sodium hydroxide solution were added to the crystalline solid so that the pH of the mixture was 13. It was stirred a further 2 hours at room temperature, then filtered off with suction and washed with water to neutrality. In this manner, 20 g (52% of theory) of 2-(4-chlorophenoxymethyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-2-butanol of melting point 84°-87° C. were obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04886892 |
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| 출처 데이터셋 | uspto-grants-1989_12 |
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| ORD ID | ord-088258d5f00a4c958780c8d5e87f8552 |
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| 출처 메모 | uspto-grants-1989_12 |
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