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HRID 273969作成日:2026年10月26日

Sulfur Dioxide → Lithium pentafluorophenylsulfenate

https://huagongshe.com/reaction/273969

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfur DioxideHCID 1119—
反応物BromopentafluorobenzeneHCID 9578—
反応物ButyllithiumHCID 178418339—
反応物HCID 178419089HCID 178419089—
溶媒Diethylether hexaneHCID 21584099—
生成物Lithium pentafluorophenylsulfenateHCID 88433932—
生成物HCID 178419089HCID 178419089—

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-dd2c81942b734e1d8f5e3bd605887ae6
出典メモuspto-grants-1995_02