GB841424A - Improvements in or relating to the production of para-diisopropylbenzene - Google Patents
Improvements in or relating to the production of para-diisopropylbenzeneInfo
- Publication number
- GB841424A GB841424A GB24371/56A GB2437156A GB841424A GB 841424 A GB841424 A GB 841424A GB 24371/56 A GB24371/56 A GB 24371/56A GB 2437156 A GB2437156 A GB 2437156A GB 841424 A GB841424 A GB 841424A
- Authority
- GB
- United Kingdom
- Prior art keywords
- para
- propylene
- cumene
- isopropylbenzene
- mol
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- SPPWGCYEYAMHDT-UHFFFAOYSA-N 1,4-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=C(C(C)C)C=C1 SPPWGCYEYAMHDT-UHFFFAOYSA-N 0.000 title 1
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 6
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- 239000000376 reactant Substances 0.000 abstract 2
- 229910015900 BF3 Inorganic materials 0.000 abstract 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/02—Monocyclic hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
- C07C2/66—Catalytic processes
- C07C2/68—Catalytic processes with halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/06—Halogens; Compounds thereof
- C07C2527/125—Compounds comprising a halogen and scandium, yttrium, aluminium, gallium, indium or thallium
- C07C2527/126—Aluminium chloride
-
- 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
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Para-di-isopropylbenzene is prepared by propylating cumene with propylene in the presence of 0.2-1.5% by weight, based on the hydrocarbon reactants, of aluminium chloride at - 80 DEG to 150 DEG C. for a time of 0.1-10 hours, the reaction being stopped before equilibrium is reached. In a preferred embodiment benzene is reacted in a first stage with undesired polyisopropylbenzenes from the second stage and propylene if required, using as catalyst aluminium chloride (2-5% by weight of hydrocarbon reactants), hydrogen fluoride, boron trifluoride, sulphuric acid or phosphoric acid under conditions such that the mol. ratio of propylating agent to benzene groups is 0.7 to 1.5:1. After separation of the catalyst, the product, or cumene separated therefrom, is propylated as above, preferably with a propylene to cumene mol. ratio of 0.8-1.5 : 1, para-di-isopropylbenzene separated by distillation and other products recycled.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB24371/56A GB841424A (en) | 1956-08-09 | 1956-08-09 | Improvements in or relating to the production of para-diisopropylbenzene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB24371/56A GB841424A (en) | 1956-08-09 | 1956-08-09 | Improvements in or relating to the production of para-diisopropylbenzene |
Publications (1)
Publication Number | Publication Date |
---|---|
GB841424A true GB841424A (en) | 1960-07-13 |
Family
ID=10210665
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB24371/56A Expired GB841424A (en) | 1956-08-09 | 1956-08-09 | Improvements in or relating to the production of para-diisopropylbenzene |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB841424A (en) |
-
1956
- 1956-08-09 GB GB24371/56A patent/GB841424A/en not_active Expired
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2775620A (en) | Production of bis (hydroxyaryl) substituted compounds | |
Ephraim et al. | Kinetic Studies of the Reaction of Phenyl Isocyanate with Alcohols in Various Solvents1 | |
GB1247451A (en) | Process for converting urethanes to isocyanates | |
GB841424A (en) | Improvements in or relating to the production of para-diisopropylbenzene | |
GB1235423A (en) | Separation of alkylation effluents | |
GB743736A (en) | Phenol production | |
US3284506A (en) | Method of dephenolizing cumene | |
US2864874A (en) | Preparation of m-and p-diisopropylbenzene | |
GB859850A (en) | Improvements in the production of 1-phenylcyclohexane-1-hydroperoxide | |
GB764338A (en) | Improvements in or relating to preparation of m- and p-diisopropylbenzenes | |
GB873614A (en) | Improvements in or relating to the production of substituted cyclohexanone peroxides | |
US2817688A (en) | Preparation of m- and p-diisopropyl-benzene | |
GB910301A (en) | Producing phenols from alkyl-aromatic hydroperoxides | |
GB948136A (en) | Preparation of condensed isopropyl silicate materials | |
GB1202687A (en) | Process for preparing phenol and acetone | |
US3985819A (en) | Process for producing alkylnaphthalenes | |
GB589072A (en) | An improved process for the production of ethyl benzene | |
US3637884A (en) | Hf alkylation of naphthalene | |
US2839591A (en) | Preparation of m-and p-diisopropylbenzene by isomerizing dhsopropylbenzenes in the prsence of aluminum chloride | |
GB763183A (en) | Improvements in or relating to preparation of m- and p-diisopropylbenzene | |
GB782084A (en) | Process for the preparation of alkyl-aryl compounds | |
US3068285A (en) | Boron compounds containing hydrocarbon radicals, hydrogen and nitrogen, and a process for the production thereof | |
GB762763A (en) | Process for the preparation of para-diisopropylbenzene | |
US3099678A (en) | Process for the preparation of trimethylborate | |
GB843032A (en) | Production of cumene hydroperoxide |