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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66229생성일: 2026년 10월 26일

Sodium hydride → 1-(2-Benzoyl-4-nitrophenyl)-3,5-pyrazole dicarboxylic acid dimethyl ester

https://huagongshe.com/reaction/66229

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3,5-dimethyl 1H-pyrazole-3,5-dicarboxylateHCID 1484491—
반응물(2-Fluoro-5-nitrophenyl)(phenyl)methanoneHCID 12377535—
반응물HCID 178418361HCID 178418361—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물1-(2-Benzoyl-4-nitrophenyl)-3,5-pyrazole dicarboxylic acid dimethyl esterHCID 12377873—

반응 단계

To a slurry of 5.3 g. (110 mmol) of 50% NaH in mineral oil in 425 ml. of dry DMF, stirred at 3° under argon, was added portionwise over a 20 minute time period, 20.26 g. (110 mmol) of 3,5-pyrazole dicarboxylic acid dimethyl ester*, maintaining a temperature of 5°-8°. When the vigorous hydrogen evolution had stopped, the ice bath was removed and the reaction allowed to warm to room temperature while stirring for 20 minutes. A solution of 24.5 g. (110 mmol) of 2-fluoro-5-nitrobenzophenone, in 100 ml. of dry DMF was added dropwise over 40 minutes and when addition was complete, the reaction was heated at 65° for 1.5 hr. After cooling, the mixture was poured over a mixture of ice and brine and extracted well with a 1:1 EtOAc:ether mixture. The combined extracts were washed with brine, dried over MgSO4 and concentrated. The crude mixture was chromatographed on silica gel using as an eluent benzene mixed with 0-100% EtOAc. The residue remaining after the solvents were evaporated was recrystallized from EtOAc/hexane to give the final product. The analytical sample was prepared by an additional recrystallization from EtOAc/hexane and was obtained as off-white needles: mp 150°-152°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04130716
출처 데이터셋uspto-grants-1978_12
ORD IDord-9bc63c263f784bf5bdf57b366e4d56bf
출처 메모uspto-grants-1978_12