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HRID 637288作成日:2026年10月27日

p-Toluenesulfonic acid → Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoate

https://huagongshe.com/reaction/637288

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物1,3-Diethyl 2-(2,3,4,5-tetrafluorobenzoyl)propanedioateHCID 13564973—
溶媒WaterHCID 962—
生成物Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 60091671.6%

反応手順

0.3 g of p-toluenesulphonic acid is added to an emulsion of 284.8 g of crude diethyl 2,3,4,5-tetrafluorobenzoyl-malonate (3) in 300 ml of water. The mixture is heated to the boil for 5 hours, while stirring thoroughly, the cold emulsion is extracted several times with methylene chloride, the combined CH2CL2 solutions are washed once with saturated NaCl solution and dried with Na2SO4, and the solvent is distilled off in vacuo. Fractionation of the residue in a fine vacuum gives 160.2 g of ethyl 2,3,4,5-tetrafluorobenzoyl-acetate (4) of boiling point 100°-110° C./0.09-0.1 mbar. Melting point 47°-49° C.

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-fefb66db3584483abd71faf62b2df084
出典メモuspto-grants-1985_12