참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium | HCID 223 | — |
| 반응물 | Imidazolium cation | HCID 444234 | — |
| 반응물 | Pyridinium | HCID 4989215 | — |
| 반응물 | Phosphonium | HCID 5460504 | — |
| 반응물 | 1467-16-9 | HCID 66617091 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Aluminum(III) Chloride | HCID 6451240 | — |
| 용매 | HCID 178462722 | HCID 178462722 | — |
| 생성물 | Ethylene | HCID 6325 | — |
| 생성물 | Ethylbenzene | HCID 7500 | — |
반응 단계
An acidic reactant also known is an acidic ionic liquid, which is a salt having a melting point of less than 100° C., can be used in Friedel-Crafts reactions as well. The systems employed to date are those formed by adding a molar excess of a Lewis acid to the halide salt of an imidazolium, pyridinium, ammonium, or phosphonium ion. One example is a mixture of Imidazolium chloride salt with a molar excess of AlCl3. These acidic chloroaluminate molten substances are used to catalyze organic reactions in place of solid AlCl3, so that the disadvantage of the low solubility of AlCl3 in most organic solvents Is minimized. Examples in the literature include the reaction of benzene and toluene with various alkyl chlorides in a mixture of 1-ethyl-3-methylimidazolium chloride ([EMIM]Cl) and AlCl3 (4 parts [EMIM]Cl/6 parts AlCl3); and the alkylation of benzene with ethylene to form ethylbenzene using a liquid catalyst phase that is a mixture of an imidazolium chloride salt having a molar excess of AlCl3 or a molar excess of GaCl3.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07691180B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-0a7bf25d698049fe8b43d8a8e76b065e |
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| 출처 메모 | uspto-grants-2010_04 |
|---|