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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376048생성일: 2026년 10월 26일

Chlorobenzene → Bis(4-chlorophenyl)iodonium trifluoromethanesulfonate

https://huagongshe.com/reaction/376048

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참여 물질

역할이름HCID투입량
반응물ChlorobenzeneHCID 7964—
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물HCID 19708102HCID 19708102—
반응물Potassium IodateHCID 23665710—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Acetic AnhydrideHCID 7918—
생성물Bis(4-chlorophenyl)iodonium trifluoromethanesulfonateHCID 223897978.6%

반응 조건

온도0 °C

반응 단계

To a mixture of 20.0 grams (178 mmol, 1 eq) of chlorobenzene in 30 mL of acetic anhydride and 19.0 grams (88.8 mmol, 0.5 eq) of potassium iodate cooled to 0° C. was added 26.7 grams (15.7 mL, 178 mmol, 1.0 eq) of triflic acid at such a rate that the reaction temperature did not exceed 0° C. The mixture was allowed to warm to room temperature slowly and stirred for 14 hours. Approximately 45 mL of water was added to the reaction mixture at 0°-20° C. followed by methylene chloride. The precipitate dissolved in the methylene chloride and the organic phase was washed with water, aqueous sodium bicarbonate, and water, and concentrated in vacuo. This material was recrystallized from a mixture of 20 mL of isopropanol and 35 mL of hexane to give 7.62 grams (8.6% yield). A second crop was obtained from the mother liquor, 2.5 grams (total yield 11.4%). The product contains less than 7% of the isomeric 2-chlorophenyl-4-chlorophenyliodonium triflate and a small amount of uncharacterized impurity.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05488147
출처 데이터셋uspto-grants-1996_01
ORD IDord-c637bad955cd4ae5bb05e77022d53f32
출처 메모uspto-grants-1996_01