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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2266344생성일: 2026년 10월 25일

Methyl triflate → ethyl 2,3-dihydro-1-methyl-3-oxo-2-phenyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/2266344

반응식

참여 물질

역할이름HCID투입량
반응물Methyl triflateHCID 9526—
반응물Ethyl 3-oxo-2-phenyl-2,3-dihydro-1h-pyrazole-4-carboxylateHCID 223722—
용매DichloromethaneHCID 6344—
생성물ethyl 2,3-dihydro-1-methyl-3-oxo-2-phenyl-1H-pyrazole-4-carboxylateHCID 1519274021.1%

반응 단계

To a solution of ethyl 3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxylate (1000 mg, 5.0 mmol) in dichloromethane (10 mL) was added methyl trifluoromethanesulfonate (1200 mg, 7.3 mmol). The red solution was stirred at room temperature. After 14 h, the mixture was partitioned between dichloromethane and NaHCO3 (sat). The aqueous was extracted with dichloromethane (2×). The combined organic was dried over Na2SO4, concentrated and purified on silica. The product was triturated with EtOAc-hexane-CHCl3 to give the pure product as crystals (260 mg, 21%). Calc'd for C12H12N2O3, 232.08; MS (ESI pos. ion) m/z: 233 (MH+). 1H NMR (400 MHz, CHLOROFORM-d): 1.36 (t, J=7.04 Hz, 3H), 3.39 (s, 3H), 4.32 (q, J=7.17 Hz, 2H), 7.32 (d, J=7.43 Hz, 2H), 7.42 (t, J=7.34 Hz, 1H), 7.50 (t, J=7.73 Hz, 2H), 7.99 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07858623B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-d851f06a3abc4c6383dc1e85a468481b
출처 메모uspto-grants-2010_12