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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

반응식

참여 물질

역할이름HCID투입량
반응물1H-1,2,4-TriazoleHCID 9257—
반응물Potassium HydroxideHCID 14797—
반응물2-tert-Butyl-2-[(4-chlorophenoxy)methyl]oxiraneHCID 12763621—
용매Dimethyl SulfoxideHCID 679—
용매TolueneHCID 1140—
생성물alpha-((4-Chlorophenoxy)methyl)-alpha-(1,1-dimethylethyl)-1H-1,2,4-triazole-1-ethanolHCID 12367652%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04886892
출처 데이터셋uspto-grants-1989_12
ORD IDord-088258d5f00a4c958780c8d5e87f8552
출처 메모uspto-grants-1989_12