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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2064915생성일: 2026년 10월 26일

Nitrogen → [5-(4-Nitro-pyrazol-1-ylmethyl)-furan-2-yl]-methanol

https://huagongshe.com/reaction/2064915

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Potassium Sodium TartrateHCID 9357—
반응물Diisobutylaluminum hydrideHCID 14487—
반응물Methyl 5-[(4-nitro-1h-pyrazol-1-yl)methyl]-2-furoateHCID 3157344—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물[5-(4-Nitro-pyrazol-1-ylmethyl)-furan-2-yl]-methanolHCID 66928816—

반응 조건

온도-78 °C

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 5-(4-nitro-pyrazol-1-ylmethyl)-furan-2-carboxylic acid methyl ester (10.0 g, 39.81 mmol) in THF (300.0 mL) was treated dropwise, at −78° C. with DiBAL (160.0 mL of a 1M solution in toluene, 160.0 mmol). The reaction mixture was stirred at −78° C. for 1.5 h and at rt for 1 h. Sat. aq. Rochelle's salt (600 mL) was added and the reaction mixture was stirred at rt for 1 h. The aq. layer was extracted with EA (2×350 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (40:60 hept-EA) gave the title compound. TLC: rf (40:60 hept-EA)=0.28. LC-MS-conditions 02: tR=0.74 min. 1H NMR (400 MHz, CDCl3) δ 2.10 (s, 1H), 4.62 (s, 2H), 5.31 (s, 2H), 6.33 (d, J=3.0 Hz, 1H), 6.47 (d, J=3.0 Hz, 1H), 8.08 (s, 1H), 8.15 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08288419B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-24315651279e4259a0eb3d21097db83e
출처 메모uspto-grants-2012_10