SU666160A1 - Method of obtaining conjugated diene hydrocarbons - Google Patents

Method of obtaining conjugated diene hydrocarbons

Info

Publication number
SU666160A1
SU666160A1 SU742038370A SU2038370A SU666160A1 SU 666160 A1 SU666160 A1 SU 666160A1 SU 742038370 A SU742038370 A SU 742038370A SU 2038370 A SU2038370 A SU 2038370A SU 666160 A1 SU666160 A1 SU 666160A1
Authority
SU
USSR - Soviet Union
Prior art keywords
conjugated diene
diene hydrocarbons
obtaining conjugated
obtaining
hydrocarbons
Prior art date
Application number
SU742038370A
Other languages
Russian (ru)
Inventor
Дилюс Лутфуллич Рахманкулов
Евгений Абрамович Кантор
Надежда Ефремовна Максимова
Семен Соломонович Злотский
Израиль Маркович Белгородский
Ефим Моисеевич Сире
Александр Григорьевич Лиакумович
Григорий Иосифович Рутман
Вера Николаевна Узикова
Original Assignee
Уфимский Нефтяной Институт
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 Уфимский Нефтяной Институт filed Critical Уфимский Нефтяной Институт
Priority to SU742038370A priority Critical patent/SU666160A1/en
Application granted granted Critical
Publication of SU666160A1 publication Critical patent/SU666160A1/en

Links

Landscapes

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

Description

ii

Изобретение огносигс  к способу получени  диеновых углеводородов, используемых в производстве сингегических каучуков .The invention of ognosigs to a method for the preparation of diene hydrocarbons used in the production of singular rubbers.

Извесген способ получени  сопр жен- 5 ных диеновых углеводородов, в том числе изопрена, дегидрированием соогвегсгвую- ишх алканов или олефинов 1 .Izvesgen is a method of producing conjugated 5 diene hydrocarbons, including isoprene, by dehydrogenating co-alkanes or alkanes or olefins 1.

Недостатками способа  вл ютс  низка  конверси  сырь , невысокий выход продук- 0 та, необходимость сложной системы разде« лени  продуктов реакции.The disadvantages of the method are the low conversion of the raw material, the low yield of the product, the need for a complex system for separating the reaction products.

Известен также способ получени  сопр  « женных диеновых углеводородов путем кон денсации олефина с альдегидом в присутст ВИИ катализатора при повышенной температуре с последующим выделением полученнь;х непредельных спиртов и их каталиги- ческим разложением при С 2.There is also known a method of obtaining conjugated diene hydrocarbons by condensation of an olefin with an aldehyde in the presence of a VIH catalyst at elevated temperature, followed by separation of the resulting unsaturated alcohols and their catalytic decomposition at C 2.

Недостатком способа  вл етс  сложност процесса, осуществл емого в двух реакто- pax с использсжанйем на каждой-стадии разных катализаторов. Значительные трудности представл ет утилизаци  побочных продуктов.The disadvantage of the process is the complexity of the process carried out in two reactors using each stage of different catalysts. Considerable difficulties are the disposal of by-products.

Целью изобретени   вл етс . упрощение процесса.The aim of the invention is. simplify the process.

Поставленна  цель достигаетс  способом получени  сопр женных диеновых углеводородов в одном реакторе при прове дении конденсации термической обработкой исходных продуктов при 12О-2ОО С в первой по ходу зоне реактора с последующим каталитическим разложением полученной смеси во второй зоне, предпочтительно , при 24О-ЗООС.This goal is achieved by the method of producing conjugated diene hydrocarbons in a single reactor by conducting thermal treatment of the initial products at 12 0 -2 2 C in the first zone of the reactor, followed by catalytic decomposition of the mixture in the second zone, preferably at 24 0 -30.

Насто щий способ позвол ет практически полностью использовать альдегид - наиболее дорогосто щий из реагенте, получать целевой продукт в одном реакторе Н упростить сасгему разделени  в очисрки целевого продукта.The present method allows the aldehyde, the most expensive of the reagent, to be used almost entirely, to obtain the desired product in a single reactor H, to simplify the separation system in the purification of the target product.

Способ предусматривает использование газообразного формальдегида, что позвол ет исключить из схемы его пронзво№ства узел получени  формалина. Кроме тоThe method involves the use of formaldehyde gas, which makes it possible to exclude the formalin production unit from its projection scheme. Besides

SU742038370A 1974-06-28 1974-06-28 Method of obtaining conjugated diene hydrocarbons SU666160A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU742038370A SU666160A1 (en) 1974-06-28 1974-06-28 Method of obtaining conjugated diene hydrocarbons

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU742038370A SU666160A1 (en) 1974-06-28 1974-06-28 Method of obtaining conjugated diene hydrocarbons

Publications (1)

Publication Number Publication Date
SU666160A1 true SU666160A1 (en) 1979-06-05

Family

ID=20589160

Family Applications (1)

Application Number Title Priority Date Filing Date
SU742038370A SU666160A1 (en) 1974-06-28 1974-06-28 Method of obtaining conjugated diene hydrocarbons

Country Status (1)

Country Link
SU (1) SU666160A1 (en)

Similar Documents

Publication Publication Date Title
US3600455A (en) Production of 4-methyl pentene-1
Olivier et al. Make aldehydes by new oxo process
DE2317525A1 (en) PROCESS FOR THE PREPARATION OF ETHYLENIC UNSATURIZED MONOMERS BY CATALYTIC OXYDEHYDRATION OF ALKYLAROMATS
SU666160A1 (en) Method of obtaining conjugated diene hydrocarbons
Negishi et al. Stereoselective synthesis of exocyclic alkenes via zirconium-promoted alkyl-diene coupling
Burkhardt et al. Carbon-Carbon bond forming reactions of organotransition metal enolate complexes
US2572724A (en) Propylene tetramer production
US2692292A (en) Oxidative dehydrogenation reactions
MacKenzie et al. Acylation-cycloalkylation. A new annelation route to Eudesmanes
US2704774A (en) Manufacture of 2, 4, 4,-trimethylphentanol
SU455086A1 (en) The method of producing cyclooctanol
US3917712A (en) Process for producing methacrolein
SU535279A1 (en) The method of producing hydroquinone
SU703519A1 (en) Method of preparing indenes
SU827477A1 (en) Method of preparing beta-methylcrotonic aldehyde
US2477312A (en) Preparation of aldehydes by steam oxidation of ethers
US2143489A (en) Manufacture of ketenes and olefines
SU717033A1 (en) Method of preparing propionic aldehyde
SU565910A1 (en) Method of obtaining tetralone-1
JPS5936892B2 (en) Method for recovering useful substances from cumene process phenol distillation residue
SU659567A1 (en) Method of obtaining 4-cyancyclohexene-1 or 1-methyl-4(3)-cyancyclohexene
SU460720A1 (en) Process for producing isoprene formaldehyde and isobutylene
SU643486A1 (en) Method of joint obtaining of oxide of cyclohexene, cyclohexenol and cyclohexenone
SU1361168A1 (en) Method of obtaining lower olefins and benzol
SU536677A1 (en) Method of obtaining tetrachlorthiophene