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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1153959생성일: 2026년 10월 27일

Hydrochloric Acid → 2-phenoxyethyl-2H-1,2,4-triazol-3(4H)-one hydrochloride

https://huagongshe.com/reaction/1153959

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물NefazodoneHCID 4449—
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물Benzene, (2-bromoethoxy)-HCID 68526—
반응물HCID 178437794HCID 178437794—
용매EthanolHCID 702—
용매AcetonitrileHCID 6342—
생성물2-phenoxyethyl-2H-1,2,4-triazol-3(4H)-one hydrochlorideHCID 13635921453%

반응 단계

Reaction in Acetonitrile With Potassium Carbonate. A mixture of 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-1H-1,2,4-triazol-3(2H)-one (15 g., 0.043 mole), phenoxyethyl bromide (8.62 g., 0.043 mole), potassium carbonate (11.9 g., 0.086 mole) and a trace of potassium iodide in 100 ml. of acetonitrile is refluxed for a 64 hr. period. The reaction mixture is filtered, the filtrate concentrated under reduced pressure and residual material taken up in ether and filtered. Concentration of the ethereal filtrate affords 18.35 g. (91%) of the free base product 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-4-(2-phenoxyethyl)-2H-1,2,4-triazol-3(4h)-one. The free base is converted to the hydrochloride in ethanol employing ethanolic hydrogenchloride and crystallized from ethanol to afford a 53% yield of analytically pure 2-[3-[4-(3-chlorophenyl)-1-piperazinyl]propyl]-5-ethyl-4-(2 -phenoxyethyl-2H-1,2,4-triazol-3(4H)-one hydrochloride, m.p. 175°-177° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04487773
출처 데이터셋uspto-grants-1984_12
ORD IDord-c3c42eef760742febe035aae7ba031d4
출처 메모uspto-grants-1984_12