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HRID 376048作成日:2026年10月23日

Chlorobenzene → Bis(4-chlorophenyl)iodonium trifluoromethanesulfonate

https://huagongshe.com/ja/reaction/376048

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorobenzeneHCID 7964—
反応物Trifluoromethanesulfonic acidHCID 62406—
反応物HCID 19708102HCID 19708102—
反応物Potassium IodateHCID 23665710—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒Acetic AnhydrideHCID 7918—
生成物Bis(4-chlorophenyl)iodonium trifluoromethanesulfonateHCID 223897978.6%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05488147
出典データセットuspto-grants-1996_01
ORD IDord-c637bad955cd4ae5bb05e77022d53f32
出典メモuspto-grants-1996_01