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HRID 273969생성일: 2026년 10월 26일

Sulfur Dioxide → Lithium pentafluorophenylsulfenate

https://huagongshe.com/reaction/273969

반응식

참여 물질

역할이름HCID투입량
반응물Sulfur DioxideHCID 1119—
반응물BromopentafluorobenzeneHCID 9578—
반응물ButyllithiumHCID 178418339—
반응물HCID 178419089HCID 178419089—
용매Diethylether hexaneHCID 21584099—
생성물Lithium pentafluorophenylsulfenateHCID 88433932—
생성물HCID 178419089HCID 178419089—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05387727
출처 데이터셋uspto-grants-1995_02
ORD IDord-dd2c81942b734e1d8f5e3bd605887ae6
출처 메모uspto-grants-1995_02