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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1296039생성일: 2026년 10월 24일

Diethyl Oxalate → Ethyl 2,4-dioxo-4-[4-(trifluoromethyl)phenyl]butanoate

https://huagongshe.com/ko/reaction/1296039

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl OxalateHCID 7268—
반응물Sodium hydrideHCID 24758—
반응물1-(4-(Trifluoromethyl)phenyl)ethan-1-oneHCID 69731—
용매DimethylformamideHCID 6228—
생성물Ethyl 2,4-dioxo-4-[4-(trifluoromethyl)phenyl]butanoateHCID 61194080%

반응 조건

온도45 °C

반응 단계

Sodium hydride (1.6 g, 63.7 mmol, 95%) was added to a solution of 1-(4-trifluoromethyl-phenyl)-ethanone (10.0 g, 53.1 mmol) and oxalic acid diethyl ester (8.7 mL, 63.7 mmol) in 75 mL dry DMF at 0° C. The reaction was allowed to come to room temperature and then heated to 45° C. for 45 minutes. The reaction was then cooled, concentrated in vacuo, and the residue taken up in EtOAc. The organic layer was then washed with 2 M HCl (1×100 mL), dried (Na2SO4) and the solvent removed in vacuo. Purification by flash column chromatography (gradient elution: 5% EtOAc/hexane to 55% EtOAc/hexane) gave the intermediate 2,4-dioxo-4-(4-trifluoromethyl-phenyl)-butyric acid ethyl ester (12.2 g, 80%) which was then taken up in EtOH and refluxed in the presence of hydroxylamine hydrochloride (10.2 g, 132.3 mmol) for 3H. The reaction was then cooled, diluted with EtOAc, washed with dilute NaHCO3, brine, dried (Na2SO4), and concentrated in vacuo. Recrystallization from EtOAc/hexane gave 5.2 g of the title compound. MS m/z 286 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07244763B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-6f389044264346f8b3e8a6144062e7ac
출처 메모uspto-grants-2007_07