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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1893723생성일: 2026년 10월 26일

Acetonitrile → 3-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-3-oxopropanenitrile

https://huagongshe.com/reaction/1893723

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물ethyl 1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylateHCID 44558860—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-3-oxopropanenitrileHCID 6666870168.2%

반응 단계

According to Scheme 7, Step 1: At −78° C., BuLi (23 mmol, 9.2 mL, 2.5M) was added dropwise to a solution of acetonitrile (21.1 mmol, 0.87 g) in THF (25 mL). The resulting mixture was stirred at this temperature for 20 minutes and then ethyl 1-(4-methoxybenzyl)-1H-pyrazole-4-carboxylate (19.2 mmol, 5.00 g) in THF (25 mL) was added. The reaction mixture was stirred at −78° C. for 1 hour and then allowed to warm up to room temperature and stirred for another 1 hour. The reaction was quenched with saturated NH4Cl aqueous solution and extracted with EtOAc (50 mL×3). The combined organic phases were dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified on combi-flash EtOAc/PE (1:15 to ˜1:5) to give 3-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-3-oxopropanenitrile (13.1 mmol, 3.33 g, 68%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08513252B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-f9eb56fe53ba43d48e791d3470649dd4
출처 메모uspto-grants-2013_08