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HRID 273970생성일: 2026년 10월 27일

Carbon Dioxide → Pentafluorobenzoic acid

https://huagongshe.com/reaction/273970

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물PentafluorobenzeneHCID 9696—
반응물ButyllithiumHCID 178418339—
반응물HCID 178419089HCID 178419089—
생성물Pentafluorobenzoic acidHCID 11770—

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-a56c8a41c2cc475db1f4ef5cf9f7b791
출처 메모uspto-grants-1995_02