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HRID 248529생성일: 2026년 10월 26일

Diethyl Malonate → Diethyl (pentafluorobenzoyl)malonate

https://huagongshe.com/reaction/248529

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl MalonateHCID 7761—
반응물Pentafluorobenzoyl chlorideHCID 75256—
반응물MagnesiumHCID 5462224—
반응물Acetone cardiceHCID 18522661—
반응물1,4-Dihydro-6-fluoro-1-(4-fluorophenyl)-4-oxo-3-[(3-thienyl)-1-piperazinyl]-3-quinolinecarboxylic acidHCID 19763550—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
용매Carbon TetrachlorideHCID 5943—
생성물Diethyl (pentafluorobenzoyl)malonateHCID 2173082299.6%

반응 단계

A 7.35 g portion of magnesium chips, 1 5 ml of carbon tetrachloride and 15 ml of absolute ethanol were added to a dry flask. A solution of 48.1 g of diethyl malonate in 30 ml of absolute ethanol and 120 ml of anhydrous ether was added dropwise over a one hour period. When addition was complete, the mixture was stirred at reflux for 3 hours then cooled to -10° C. with dry ice/acetone. A solution of 70 g of pentafluorobenzoyl chloride in 120 ml of ether was added over 2 hours, maintaining the temperature at not more than -5° C. The mixture was then stirred overnight at room temperature, partially evaporated, cooled in crushed ice and an ice cold solution of 7.5 ml of concentrated sulfuric acid in 300 ml of Water was added at a rate such that the internal temperature did not go above 5° C. The mixture was extracted several times with ether, the extracts combined, washed with saturated sodium chloride, dried and concentrated, giving 106 g of (pentafluorobenzoyl)propanedioic acid, diethyl ester as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210193
출처 데이터셋uspto-grants-1993_05
ORD IDord-df893f5365db42c693d25be937aa80c0
출처 메모uspto-grants-1993_05