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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273969Erstellt: 25. Oktober 2026

Sulfur Dioxide → Lithium pentafluorophenylsulfenate

https://huagongshe.com/reaction/273969

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfur DioxideHCID 1119—
EduktBromopentafluorobenzeneHCID 9578—
EduktButyllithiumHCID 178418339—
EduktHCID 178419089HCID 178419089—
LösungsmittelDiethylether hexaneHCID 21584099—
ProduktLithium pentafluorophenylsulfenateHCID 88433932—
ProduktHCID 178419089HCID 178419089—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05387727
Quelldatensatzuspto-grants-1995_02
ORD IDord-dd2c81942b734e1d8f5e3bd605887ae6
Quellennotizuspto-grants-1995_02