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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1386962생성일: 2026년 10월 27일

Hydrochloric Acid → 5-(4-Difluoromethoxy-phenyl)-3-(3-[1,3]dioxolan-2-yl-phenyl)-1H-[1,2,4]triazole

https://huagongshe.com/reaction/1386962

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium ethoxideHCID 2723922—
반응물4-(Difluoromethoxy)benzonitrileHCID 2736990—
반응물SodiumHCID 5360545—
반응물3-(1,3-Dioxolan-2-yl)benzohydrazideHCID 69829968—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
생성물5-(4-Difluoromethoxy-phenyl)-3-(3-[1,3]dioxolan-2-yl-phenyl)-1H-[1,2,4]triazoleHCID 2118033462%

반응 단계

To a solution of 4-(difluoromethoxy)benzonitrile (5 g, 30 mmol) in ethanol at 4° C. was bubbled dry HCl(g) for 3 h. The resulting mixture was stoppered and kept at 4° C. for 65 h. Ether (40 ml) was then added with ultrasonication to precipitate the imidate hydrochloride salt, which was washed twice with dry ether (40 ml) and then dried under vacuum (0.05 mmHg) at 20° C. To a solution of imidate hydrochloride salt (1 g, 4 mmol) in ethanol (15 ml) was added sodium ethoxide solution dropwise (sodium: 98 mg, 4 mmol in 5 ml of dry ethanol) at room temperature. The reaction was allowed to stir for a further 30 min then 3-[1,3]Dioxolan-2-yl-benzoic acid hydrazide was added (824 mg, 4 mmol) and the mixture was heated to reflux for 22 h until the starting materials were consumed. The reaction mixture was evaporated to dryness and chromatographed over SiO2 (Merck 230-400 mesh) eluting with EtOAc/nHexane (3:7), the product fractions were combined and evaporated to afford the title compound as a white solid (885 mg, 62% yield), MS: m/e=359.1 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06265426B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-136f5332684a4bc5a812e485ebc51524
출처 메모uspto-grants-2001_07