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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 638678생성일: 2026년 10월 25일

Ammonium → Ethylene

https://huagongshe.com/reaction/638678

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참여 물질

역할이름HCID투입량
반응물AmmoniumHCID 223—
반응물Imidazolium cationHCID 444234—
반응물PyridiniumHCID 4989215—
반응물PhosphoniumHCID 5460504—
반응물1467-16-9HCID 66617091—
용매BenzeneHCID 241—
용매TolueneHCID 1140—
용매Aluminum(III) ChlorideHCID 6451240—
용매HCID 178462722HCID 178462722—
생성물EthyleneHCID 6325—
생성물EthylbenzeneHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691180B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-0a7bf25d698049fe8b43d8a8e76b065e
출처 메모uspto-grants-2010_04