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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1191175생성일: 2026년 10월 27일

Methylhydrazine → 5-tert-Butyl-4-methoxy-2-methyl-2H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1191175

반응식

참여 물질

역할이름HCID투입량
반응물MethylhydrazineHCID 6061—
반응물Boron trifluoride etherateHCID 8000—
반응물Ethyl 5,5-dimethyl-2,4-dioxohexanoateHCID 83403—
반응물Bis(trifluoroacetoxy)iodobenzeneHCID 102317—
용매MethanolHCID 887—
생성물5-tert-Butyl-4-methoxy-2-methyl-2H-pyrazole-3-carboxylic acid ethyl esterHCID 67411723—

반응 단계

[Bis(trifluoroacetoxy)iodo]benzene (430 mg, 1.00 mmol) was dissolved in anhydrous MeOH (4 mL), the resulting solution was stirred at room temperature for 3 min. BF3.OEt2 (0.123 mL, 1.00 mmol) was then added via syringe. Ethyl trimethylacetopyruvate (200 mg, 1.00 mmol) was added dropwise via syringe and the resulting mixture was stirred at room temperature for 12 h. The solvent was removed under reduced pressure and the resulting residue was dissolved in dry EtOH (2 mL). CH3NHNH2 (52.6 μL, 1.00 mmol) was added via syringe and the resulting mixture was stirred at 80° C. for 8 h. The solvent was removed under reduced pressure and the resulting residue was chromatographed on a 24-g SiO2 pre-packed column eluting with 0:1-3:7 EtOAc/hexanes to yield 5-tert-butyl-4-methoxy-2-methyl-2H-pyrazole-3-carboxylic acid ethyl ester. 1H-NMR (400 MHz, CDCl3) δ: 4.39 (q, J=7.1 Hz, 2H), 4.03 (s, 3H), 3.83 (s, 3H), 1.42 (t, J=7.2 Hz, 3H), 1.34 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08680098B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-80a778eefe554284b542a2462b94bd05
출처 메모uspto-grants-2014_03