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SU384813A1 - METHOD OF OBTAINING ACYLATED AROMATIC HYDROCARBONS - Google Patents

METHOD OF OBTAINING ACYLATED AROMATIC HYDROCARBONS

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Publication number
SU384813A1
SU384813A1 SU1385530A SU1385530A SU384813A1 SU 384813 A1 SU384813 A1 SU 384813A1 SU 1385530 A SU1385530 A SU 1385530A SU 1385530 A SU1385530 A SU 1385530A SU 384813 A1 SU384813 A1 SU 384813A1
Authority
SU
USSR - Soviet Union
Prior art keywords
aromatic hydrocarbons
acylated aromatic
catalyst
obtaining
obtaining acylated
Prior art date
Application number
SU1385530A
Other languages
Russian (ru)
Inventor
Л. И. Ковалевска Днепропетровский химико технологический институт Ф. Э. Дзержинского Н. К. Мощинска А. М. Каратеев
Original Assignee
Авторы изобретени витель
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Авторы изобретени витель filed Critical Авторы изобретени витель
Priority to SU1385530A priority Critical patent/SU384813A1/en
Application granted granted Critical
Publication of SU384813A1 publication Critical patent/SU384813A1/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Description

Изобретение относитс  к способу получени  ацилированных ароматических углеводо (родов.This invention relates to a method for producing acylated aromatic carbohydrates (genera.

Известен способ получени  ацилированных ароматических углеводородов при взаимодействии ароматических углеводородов с ацилхлоридами в присутствии катализатора - галогенидов металлов, например AlCls.A method of producing acylated aromatic hydrocarbons by reacting aromatic hydrocarbons with acyl chlorides in the presence of a catalyst — metal halides, such as AlCls, is known.

Одна.ко выход целевого продукта недостаточно высок.However, the yield of the target product is not high enough.

С целью .повышени  выхода целевого продукта предлагаетс  в качестве катализатора использовать комплексное соединение на основе хлоридов металлов и солей четырехзамещенного афгмони  общей формулы.In order to increase the yield of the target product, it is proposed to use as a catalyst a complex compound based on metal chlorides and salts of tetra-substituted afmonium of the general formula.

МеС1„ R4NC1-A, гдеМеС1 „R4NC1-A, where

Вз то 0,1 лголь .катали.з.а1р.ра..,.It is 0.1 lgol. Catal.z.a1r.ra ..,.

п.ри n Q,5-2,0 моль или MeCU, где МеСи А1.С1з, FeCls, ZnCb; R - углеводородный радикал. p.ri n Q, 5-2.0 mol or MeCU, where MeCu A1. Cl3, FeCls, ZnCb; R is a hydrocarbon radical.

Пример. 1. Ароматический углеводород, ащилхлорид и катализатор, вз тые в мол рном отношении 10 : 1 : 0,05 или 10 : 1 : 0,1, нагревают с обратнЫ|М холодильником с поглощением выдел ющегос  хлористого водорода. По окончании выделени  хлористого водорода или заданного времени реакции реакционную смесь сливают с катализатора, .промывают водой дл  удалени  следов катализатора И разгон ют, отдел   «епрореагировавшие исходные вещества и продукты . Выход продуктов реакщиИ и их характеристика приведены в та1бли1це.Example. 1. The aromatic hydrocarbon, acetyl chloride and catalyst, taken in a molar ratio of 10: 1: 0.05 or 10: 1: 0.1, are heated in reverse to an M condenser to absorb the released hydrogen chloride. At the end of the evolution of hydrogen chloride or a predetermined reaction time, the reaction mixture is poured from the catalyst, washed with water to remove traces of the catalyst. And dispersed, the "unreacted starting materials and products" are separated. The yield of the products of reactants and their characteristics are given in the table.

Пример 2. Провод т опыт, как в примере 1, и получают кетоны с ВЬРХОДОМ 70-80%. Результаты нексторык опытов (приведены в таблице.Example 2. The experiment was carried out as in Example 1, and ketones with a VIROMPUT of 70-80% were obtained. The results nekstoryk experiments (listed in the table.

Предмет изобретени Subject invention

Способ получени  ащилированных аромати1чеоких углеводородов путем взаимодействи  ароматических углеводородов с ацилхлоридами в присутствии катализатора, отличающийс  тем, что, с .целью повышени  выхода целевого продукта, в качестве катализатора .используют комплексное соединение на осно .ве хлоридов металлов и солей четырехзамещенного аммони  об:щей формулы MeCl.v - R4NC1 - А, где А л НС1 при ,5-2,0 моль или MeCli, где MeCU AlCla, FeCU, ZnCb; R - углеводородный радикал.A method of producing an optimized aromatic hydrocarbon by reacting aromatic hydrocarbons with acyl chlorides in the presence of a catalyst, characterized in that, in order to increase the yield of the target product, a complex compound based on metal chlorides and salts of tetra-substituted ammonium of the general formula MeCl is used as a catalyst. .v - R4NC1 - A, where A is l HC1 at, 5-2.0 mol or MeCli, where MeCU AlCla, FeCU, ZnCb; R is a hydrocarbon radical.

SU1385530A 1969-12-15 1969-12-15 METHOD OF OBTAINING ACYLATED AROMATIC HYDROCARBONS SU384813A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1385530A SU384813A1 (en) 1969-12-15 1969-12-15 METHOD OF OBTAINING ACYLATED AROMATIC HYDROCARBONS

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1385530A SU384813A1 (en) 1969-12-15 1969-12-15 METHOD OF OBTAINING ACYLATED AROMATIC HYDROCARBONS

Publications (1)

Publication Number Publication Date
SU384813A1 true SU384813A1 (en) 1973-05-29

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Application Number Title Priority Date Filing Date
SU1385530A SU384813A1 (en) 1969-12-15 1969-12-15 METHOD OF OBTAINING ACYLATED AROMATIC HYDROCARBONS

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SU (1) SU384813A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4814508A (en) * 1984-10-11 1989-03-21 Raychem Corporation Friedel-crafts preparation of aromatic ketones
CN105085303A (en) * 2015-06-26 2015-11-25 丰益特种化学(连云港)有限公司 Quaternary ammonium salt compound, preparation method therefor and use thereof as catalyst in acyl chloride preparation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4814508A (en) * 1984-10-11 1989-03-21 Raychem Corporation Friedel-crafts preparation of aromatic ketones
CN105085303A (en) * 2015-06-26 2015-11-25 丰益特种化学(连云港)有限公司 Quaternary ammonium salt compound, preparation method therefor and use thereof as catalyst in acyl chloride preparation

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