戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 637287作成日:2026年10月27日

Sulfuric Acid → 1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioate

https://huagongshe.com/reaction/637287

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Diethyl MalonateHCID 7761—
反応物2,3,4,5-Tetrafluorobenzoyl chlorideHCID 2733689—
反応物MagnesiumHCID 5462224—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
溶媒Carbon TetrachlorideHCID 5943—
生成物1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioateHCID 1356497399.7%

反応手順

24.g of magnesium turnings are suspended in 50 ml of anhydrous ethanol. 5 ml of carbon tetrachloride are added, and, when the reaction has started, a mixture of 160 g of diethyl malonate, 100 ml of absolute ethanol and 400 ml of anhydrous toluene is added dropwise at 50°-60° C. Thereafter, the mixture is heated to 50°-60° C. for a further hour, and cooled to -5° C. to -10° C. with dry ice acetone, and a solution of 212.5 g of 2,3,4,5-tetrafluorobenzoyl chloride (1) in 80 ml of absolute toluene is slowly added dropwise at this temperature. The mixture is stirred for 1 hour at 0° to -5° C., and is allowed to reach room temperature overnight, and a mixture of 400 ml of ice water and 25 ml of concentrated sulphuric acid is allowed to run in whilst cooling with ice. The phases are separated, and extraction with toluene is repeated twice. The combined toluene solutions are washed with saturated NaCl solution and dried with Na2SO4, and the solvent is stripped off in vacuo. 335 g of diethyl 2,3,4,5-tetra-fluorobenzoylmalonate (3) are obtained as a crude product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04556658
出典データセットuspto-grants-1985_12
ORD IDord-c1be0238ed7b471b99e4c73dbf8161fe
出典メモuspto-grants-1985_12