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Methyl 3,3,3-trifluoro-2-oxopropanoate → HCID 44139823, 화합물

HRID 424927
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인쇄 미리보기

반응식

HRID 424927 반응식
[CH3:1][C:2]1[NH:3][N:4]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)[C:5](=[O:7])[CH:6]=1.[F:15][C:16]([F:24])([F:23])[C:17](=[O:22])[C:18]([O:20][CH3:21])=[O:19]>C(Cl)(Cl)Cl>[CH3:21][O:20][C:18](=[O:19])[C:17]([OH:22])([C:16]([F:24])([F:23])[F:15])[C:6]1[C:5](=[O:7])[N:4]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)[NH:3][C:2]=1[CH3:1]
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참가 물질

4

반응물 2

HCID 2734931Methyl 3,3,3-trifluoro-2-oxopropanoateHCID 27368983-Methyl-1-(4-methylphenyl)-1H-pyrazol-5-ol

생성물 1

HCID 44139823HCID 44139823, 화합물

시약·촉매·용매 1

HCID 6212Chloroform용매

반응 조건

온도
80 °C

실험 절차

To a chloroform solution (5 ml) of 3-methyl-1-(4-methylphenyl)-5-pyrazolone (94 mg, 0.5 mmol), methyl trifluoropyruvate (78 mg, 0.5 mmol) was added at room temperature and the mixture was stirred at 80° C. for 2 hours. After removing the solvent under reduced pressure, the title compound was obtained as a pale yellow solid (172 mg).

후처리

  1. customAfter removing the solvent under reduced pressure

출처 및 근거

ORD 기록
ord-036b44fd43bd4eb6a33399ca900eb9ef
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106086B2

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