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HRID 248529作成日:2026年10月25日

Diethyl Malonate → Diethyl (pentafluorobenzoyl)malonate

https://huagongshe.com/reaction/248529

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl MalonateHCID 7761—
反応物Pentafluorobenzoyl chlorideHCID 75256—
反応物MagnesiumHCID 5462224—
反応物Acetone cardiceHCID 18522661—
反応物1,4-Dihydro-6-fluoro-1-(4-fluorophenyl)-4-oxo-3-[(3-thienyl)-1-piperazinyl]-3-quinolinecarboxylic acidHCID 19763550—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
溶媒Carbon TetrachlorideHCID 5943—
生成物Diethyl (pentafluorobenzoyl)malonateHCID 2173082299.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05210193
出典データセットuspto-grants-1993_05
ORD IDord-df893f5365db42c693d25be937aa80c0
出典メモuspto-grants-1993_05