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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238358생성일: 2026년 10월 25일

Ethanol → 1-methyl-5-(2-phenylethenyl)-1H-pyrazole

https://huagongshe.com/reaction/238358

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물beta-BromostyreneHCID 7667—
반응물Potassium CarbonateHCID 11430—
반응물1-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 4912908—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-methyl-5-(2-phenylethenyl)-1H-pyrazoleHCID 7140198774.5%

반응 조건

온도75 °C

반응 단계

Under a nitrogen atmosphere, a mixture of 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (1.50 g), β-bromostyrene (1.45 g), bis(triphenylphosphine)palladium(II) dichloride (506 mg), potassium carbonate (1.30 g), ethanol (3.8 mL) and dimethylformamide (7.5 mL) was stirred at 75° C. for 6 hours. Thereafter, 13-bromostyrene (1.45 g) was further added to the reaction solution, and the obtained solution was then stirred at 75° C. for 4 hours. Subsequently, the reaction solution was diluted with ethyl acetate, and was then washed with water. The organic layer was dried over anhydrous magnesium sulfate, and was then concentrated under a reduced pressure. The residue was purified by column chromatography (silica gel 60N, hexane:ethyl acetate=4:1 to 3:1), so as to obtain the title compound (990 mg) in the form of a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642626B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-cdf1f42d84c94674be51e5c49efc0fb6
출처 메모uspto-grants-2014_02