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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1381139생성일: 2026년 10월 24일

Triethylamine → 2,4-difluoro-alpha-(1H-1,2,4-triazol-1-yl)acetophenone hydrochloride

https://huagongshe.com/ko/reaction/1381139

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1H-1,2,4-TriazoleHCID 9257—
반응물2-Chloro-1-(2,4-difluorophenyl)ethanoneHCID 588083—
용매Ethyl AcetateHCID 8857—
생성물2,4-difluoro-alpha-(1H-1,2,4-triazol-1-yl)acetophenone hydrochlorideHCID 1305969941.6%

반응 단계

To a mixture of 1,2,4-triazole (30.4 g, 0.44M) and triethylamine (15.1 g, 0.15M) in refluxing ethyl acetate (186 ml) was added a solution of 2-chloro-2',4'-difluoroacetophenone (38.1 g, 0.2M) in ethyl acetate (80 ml). The mixture was refluxed for six hours then cooled to room temperature and the insolubles were removed by filtration. The filtrate was washed with water (2×200 ml) and then the solvent was removed by distillation at reduced pressure. The crude product was dissolved in ethyl acetate (150 ml) then 25% w/v HCl gas in isopropanol was added. The mixture was granulated at 0° C. for one hour and then the solid was collected by filtration and dried to give the title compound (21.6 g, 40%), melting point 167°-170° C. IR (KBr) and nmr (DMSO) were consistent with the desired structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04585778
출처 데이터셋uspto-grants-1986_04
ORD IDord-5e958b564b884fa9a78e8f5bdac9abc4
출처 메모uspto-grants-1986_04