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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273969Generated: October 25, 2026

Sulfur Dioxide → Lithium pentafluorophenylsulfenate

https://huagongshe.com/reaction/273969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
ReactantBromopentafluorobenzeneHCID 9578—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178419089HCID 178419089—
SolventDiethylether hexaneHCID 21584099—
ProductLithium pentafluorophenylsulfenateHCID 88433932—
ProductHCID 178419089HCID 178419089—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387727
Source datasetuspto-grants-1995_02
ORD IDord-dd2c81942b734e1d8f5e3bd605887ae6
Source noteuspto-grants-1995_02