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HRID 981128作成日:2026年10月26日

Sulfuric Acid → Diethyl (2,4-dichloro-3,6-difluorobenzoyl)-malonate

https://huagongshe.com/reaction/981128

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Propanedioic acid, monoethyl esterHCID 3595298—
反応物MagnesiumHCID 5462224—
反応物2,4-Dichloro-3,6-difluorobenzoyl chlorideHCID 15070033—
反応物Acetone cardiceHCID 18522661—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
溶媒Carbon TetrachlorideHCID 5943—
生成物Diethyl (2,4-dichloro-3,6-difluorobenzoyl)-malonateHCID 15070034—

反応条件

温度70 °C

反応手順

2.1 g of magnesium filings are suspended in 5 ml of anhydrous ethanol. 0.5 ml of carbon tetrachloride is added and, when the reaction has started, a mixture of 14 g of ethyl malonate, 10 ml of absolute ethanol and 41 ml of toluene is added dropwise. The mixture is then heated at 70° C. for a further 1.5 hours and cooled to -5° C. to -10° C. with acetone/dry ice, and a solution of 21.5 g of 2,4-dichloro-3,6-difluorobenzoyl chloride in 30 ml of toluene is slowly added dropwise at this temperature. The mixture is stirred at 0° C. for 1 hour and allowed to come to room temperature overnight, and a mixture of 35 ml of ice-water and 5 ml of concentrated sulphuric acid is allowed to run in, while cooling with ice. The phases are separated and subsequent extraction is carried out twice with toluene. The combined toluene solutions are washed once with saturated sodium chloride solution and dried with Na2SO4 and the solvent is stripped off in vacuo. 34.7 g of diethyl (2,4-dichloro-3,6-difluorobenzoyl)-malonate are obtained as a crude product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04990517
出典データセットuspto-grants-1991_02
ORD IDord-fec1db9c27ab4f3db8c0b32b3d18e969
出典メモuspto-grants-1991_02