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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 415932생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/415932

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, 3 H), 3.39 (s, 3 H), 4.32 (q, J=7.17 Hz, 2 H), 7.32 (d, J=7.43 Hz, 2 H), 7.42 (t, J=7.34 Hz, 1 H), 7.50 (t, J=7.73 Hz, 2 H), 7.99 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088794B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-0367d78ef07b45d5a091461dfa2dc7ed
출처 메모uspto-grants-2012_01