SU670326A1 - Catlyst for alkylation of benzene with propylene - Google Patents
Catlyst for alkylation of benzene with propyleneInfo
- Publication number
- SU670326A1 SU670326A1 SU782580515A SU2580515A SU670326A1 SU 670326 A1 SU670326 A1 SU 670326A1 SU 782580515 A SU782580515 A SU 782580515A SU 2580515 A SU2580515 A SU 2580515A SU 670326 A1 SU670326 A1 SU 670326A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- benzene
- propylene
- alkylation
- catlyst
- fraction
- Prior art date
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Description
етс (расход хлористого алюмини на тонну кумола составл ет 15-20 кг).(consumption of aluminum chloride per ton of cumene is 15-20 kg).
Прнмер. В колбу с мешалкой, обратным холодильником и термометром ввод т 26,67 г 0,2 М А1С1з и 44,48 г 0,15 М октаметилциклотетрасилоксана . Смесь нагревают при перемешивании 10 ч при температуре 120°С. По окончании реакции продукты реакции , представл ющие собой смесь кристаллов с жидкой фазой, были расфракционированы в вакууме. При этом получают 17,53 г фракции с температурой кипени 30-116°С (10 мм) и 34,24 г фракции с температурой кипени 116-193°С (10 мм), полностью закристаллизовавшейс в приемнике . После вторичного тш,ательного фракционировани и еублимации кристаллической фракции получают 28,12 г белых кристаллов с температурой плавлени 152-Prnmer. 26.67 g of 0.2 M AlCl3 and 44.48 g of 0.15 M octamethylcyclotetrasiloxane are introduced into the flask with a stirrer, a reflux condenser and a thermometer. The mixture is heated with stirring for 10 hours at a temperature of 120 ° C. At the end of the reaction, the reaction products, which are a mixture of crystals with a liquid phase, were disfractionated in vacuum. 17.53 g of a fraction with a boiling point of 30-116 ° C (10 mm) and 34.24 g of a fraction with a boiling point of 116-193 ° C (10 mm), completely crystallized in the receiver, are obtained. 28.12 g of white crystals with a melting point of 152- are obtained after the secondary solid phase fractionation and elimation of the crystalline fraction.
153°С, легко сублимирующихс под вакуумом . Вещество хорощо раствор етс в воде , в спирте и в серном эфире, в бензоле растворимо только при нагревании. Дл свежесиптезпрованпого вещества сделан элементный анализ: С8П240бС15Si4Al3 .153 ° C, easily subliminated under vacuum. The substance is horosho soluble in water, in alcohol and in sulfuric ether, in benzene it is soluble only when heated. For freshly synthesized substance, elemental analysis was performed: S8P240bS15Si4Al3.
Найдено, %: С 16,63, 16,67; Si 20,24, 19,98; Н 4,35, 4, 28; С1 29,92, 29,59; А 12,55, 13,09.Found,%: C 16.63, 16.67; Si 20.24, 19.98; H 4.35, 4, 28; C1 29.92, 29.59; A 12.55, 13.09.
Вычислено, %: С 16,37; Н 4,12; С1 30,21; Si 19,14; А1 13,79.Calculated,%: C 16.37; H 4.12; C1 30.21; Si 19.14; A1 13.79.
Приготовлеппый таким способом катализатор испытывают на каталитическую активность в реакции алкилировани бензола пропиленом.Prepared in this way, the catalyst is tested for catalytic activity in the alkylation reaction of benzene with propylene.
Результаты исследовани представлены в таблице.The results of the study are presented in the table.
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU782580515A SU670326A1 (en) | 1978-02-15 | 1978-02-15 | Catlyst for alkylation of benzene with propylene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU782580515A SU670326A1 (en) | 1978-02-15 | 1978-02-15 | Catlyst for alkylation of benzene with propylene |
Publications (1)
Publication Number | Publication Date |
---|---|
SU670326A1 true SU670326A1 (en) | 1979-06-30 |
Family
ID=20749239
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU782580515A SU670326A1 (en) | 1978-02-15 | 1978-02-15 | Catlyst for alkylation of benzene with propylene |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU670326A1 (en) |
-
1978
- 1978-02-15 SU SU782580515A patent/SU670326A1/en active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0230250A3 (en) | Process for the preparation of 5-hydroxymethylfurfural, including a crystalline product, using exclusively water as solvent | |
ES2003076T3 (en) | PROCEDURE FOR OBTAINING PURE DIMETILETER. | |
SU670326A1 (en) | Catlyst for alkylation of benzene with propylene | |
SU734182A1 (en) | Method of producing secondary butanol | |
Barclay et al. | ortho-DIQUATERNARY AROMATIC COMPOUNDS: I. THE SYNTHESIS OF ortho-DITERTIARYBUTYLBENZENE. SOME REACTIONS OF SIDE CHAIN SUBSTITUTED DERIVATIVES | |
KR970000138B1 (en) | Process for the preparation of alkyl 3-alkoxypropionates | |
US4804788A (en) | Preparation process of 4,4-dihydroxybiphenyl | |
FR2444657A1 (en) | PROCESS FOR THE PREPARATION OF METHYL-NONYL-ACETALDEHYDE | |
SU798102A1 (en) | Method of combined preparation of n,n,n-tribenzylhexahydrotriazine-1,3,5 and n-methylbenzylamino-n'-benzyliminomethylene | |
SU582753A3 (en) | Method of preparing acetophenone | |
SU819098A1 (en) | Method of preparing 2-methylbenzimidazole | |
SU520357A1 (en) | The method of obtaining 2,2,6,6-tetramethyl-4-oxopiperidine | |
US4451662A (en) | Process for preparing 2,3-dihydro-2,2-dimethyl-7-hydroxybenzofuran | |
SU869290A1 (en) | Bis-aryl-o-carborane as intermediate product in synthesis of polymers of polyphenylene type | |
SU505648A1 (en) | Method of producing methylphenyldichlorosilane | |
US4117243A (en) | Preparation of o-benzylphenol | |
Orchin et al. | The Isomerization of Dicyclohexy1 | |
JPS5634661A (en) | Preparation of 1,4-bis dicyanomethylene cyclohexane | |
SU785325A1 (en) | Method of preparing polymethylene | |
SU413134A1 (en) | ||
JPS5826889B2 (en) | Manufacturing method of resorcinol | |
SU1085970A1 (en) | Process for preparing 2-tert-butylphenol | |
DK416081A (en) | METHOD FOR PREPARING 3-BROMO-4-FLUOROBENOIC ACID | |
RU2049087C1 (en) | Process for preparing 2,2-methylene-bis-(4-methyl-6-tert-butylphenol) | |
SU657007A1 (en) | Method of obtaining tret-butylbenzol |