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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 890184생성일: 2026년 10월 24일

2-Acetylbutyrolactone → 3-((E)-1-[3-Methyl-1-(2,4,6-trichlorophenyl)-1H-5-pyrazolyl]aminoethylidene)tetrahydro-2-furanone

https://huagongshe.com/ko/reaction/890184

반응식

참여 물질

역할이름HCID투입량
반응물2-AcetylbutyrolactoneHCID 10601—
반응물3-Methyl-1-(2,4,6-trichlorophenyl)-1H-pyrazol-5-amineHCID 2060032—
용매EthanolHCID 702—
생성물3-((E)-1-[3-Methyl-1-(2,4,6-trichlorophenyl)-1H-5-pyrazolyl]aminoethylidene)tetrahydro-2-furanoneHCID 2224950749.7%

반응 단계

3-Amino-2-(2,4,6-trichlorophenyl)-5-methylpyrazole (1 g, 3.62 mmol) was dissolved in ethanol (10 mL). α-Acetyl-γ-butyrolactone (0.409 mL, 3.80 mmol) was added, followed by heating under reflux for two days. After ethanol was evaporated, the residue was purified by silica gel column chromatography (10% ethyl acetate/hexane), to give the title compound (700 mg, 1.80 mmol) as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06995163B2
출처 데이터셋uspto-grants-2006_02
ORD IDord-4a991ae114bf42a28a6945ad5afb4faa
출처 메모uspto-grants-2006_02