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HRID 2061315作成日:2026年10月25日
Bis(4-tert-butylphenyl)iodanium hydrogen sulfate → Bis(4-tert-butylphenyl)iodonium 3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropane-1-sulfonate
https://huagongshe.com/reaction/2061315
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bis(4-tert-butylphenyl)iodanium hydrogen sulfate | HCID 20205689 | — |
| 反応物 | Sodium 3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropane-1-sulfonate | HCID 59445712 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Bis(4-tert-butylphenyl)iodonium 3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropane-1-sulfonate | HCID 86644258 | 72% |
反応手順
Bis(4-tert-butylphenyl)iodonium hydrogen sulfate (0.02 mole equivalent) prepared in Synthesis Example 1-6, 0.024 mole equivalent of the aqueous solution of sodium 3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropane-1-sulfonate prepared in Synthesis Example 1-9, and 70 g of methylene chloride were mixed and agitated at room temperature for 1 hour. After the agitation, the organic layer was separated, washed by water, and then concentrated under reduced pressure. The residue was recrystallized by adding diisopropyl ether, and then the obtained crystals were recovered and dried to obtain the intended bis(4-tert-butylphenyl)iodonium 3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropane-1-sulfonate (9.4 g of white crystals (yield 72%)). The structure of the intended product is shown below.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08283104B2 |
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| 出典データセット | uspto-grants-2012_10 |
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| ORD ID | ord-22c4a858fb624b2ea64e2af2aa81e8bb |
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| 出典メモ | uspto-grants-2012_10 |
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