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HRID 273970作成日:2026年10月27日

Carbon Dioxide → Pentafluorobenzoic acid

https://huagongshe.com/reaction/273970

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物PentafluorobenzeneHCID 9696—
反応物ButyllithiumHCID 178418339—
反応物HCID 178419089HCID 178419089—
生成物Pentafluorobenzoic acidHCID 11770—

反応手順

Up to now, several synthetic reactions for pentafluorophenyl alkali metal salt are known. For example, a method of producing pentafluorophenyllithium through bromine-metal exchange reaction using relatively expensive bromopentafluorobenzene as a starting raw material for a source of pentafluorophenyl group and butyllithium is already known. For example, in Synthesis of Fluoroorganic Compounds, p. 190, Springer-Verlag (1985), pentafluorophenyllithium is prepared in diethylether-hexane at -70° C. and is reacted with sulfur dioxide to give lithium pentafluorophenylsulfenate with 94% yield. Also, a method of producing pentafluorophenyllithium through hydrogen-metal exchange reaction using pentafluorobenzene as a starting raw material for a source of pentafluorophenyl group and butyllithium is already known. For example, in J. Org. Chem., 29, 2385 (1964), pentafluorophenyllithium prepared from pentafluorobenzene and butyllithium is reacted with carbon dioxide gas to give pentafluorobenzoic acid wherein the reaction yield is unknown, but the purification yield, depending on reaction solvent system, is 68% in diethylether-hexane system, 80.9% in diethylether type and 82% in diethylether-tetrahydrofuran system respectively.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387727
出典データセットuspto-grants-1995_02
ORD IDord-a56c8a41c2cc475db1f4ef5cf9f7b791
出典メモuspto-grants-1995_02