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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251916생성일: 2026년 10월 26일

4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedione → 1-(2-Chlorophenyl)-5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazole

https://huagongshe.com/reaction/251916

반응식

참여 물질

역할이름HCID투입량
반응물4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedioneHCID 67594—
반응물2-Chlorophenylhydrazine hydrochlorideHCID 443287—
반응물Sodium AcetateHCID 517045—
용매Acetic AcidHCID 176—
생성물1-(2-Chlorophenyl)-5-(furan-2-yl)-3-(trifluoromethyl)-1H-pyrazoleHCID 5745823693.7%

반응 조건

온도60 °C

반응 단계

To a mixture of 12.96 g of 4,4,4-trifluoro-1-(2-furyl)-1,3-butanedione, 8.56 g of sodium acetate and 40 ml of acetic acid was added 11.26 g of 2-chlorophenylhydrazine hydrochloride at room temperature. The mixture was stirred at 60° C. for 1 hour, and concentrated under reduced pressure. After the reaction mixture was concentrated under reduced pressure and water was poured into the residue, the mixture was extracted with chloroform three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to obtain 18.43 g of 1-(2-chlorophenyl)-5-(2-furyl)-3-trifluoromethyl-1H-pyrazole of the formula:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07867949B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-f9b7dcad17d94a3ab65ed3021aada78c
출처 메모uspto-grants-2011_01