GB589015A - Improvements in the manufacture of styrene and derivatives of styrene - Google Patents

Improvements in the manufacture of styrene and derivatives of styrene

Info

Publication number
GB589015A
GB589015A GB653545A GB653545A GB589015A GB 589015 A GB589015 A GB 589015A GB 653545 A GB653545 A GB 653545A GB 653545 A GB653545 A GB 653545A GB 589015 A GB589015 A GB 589015A
Authority
GB
United Kingdom
Prior art keywords
phenyl methyl
methyl carbinol
hydroquinone
styrene
derivatives
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
Application number
GB653545A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB653545A priority Critical patent/GB589015A/en
Publication of GB589015A publication Critical patent/GB589015A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/20Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
    • C07C1/24Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms by elimination of water
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/35Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/02Boron or aluminium; Oxides or hydroxides thereof
    • C07C2521/04Alumina

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)

Abstract

Styrene or its substitution derivatives are prepared by heating phenyl methyl carbinol or a substitution derivative thereof in vapour phase under a pressure below 300 mm. in contact with a dehydration catalyst. Substitution derivatives include alkyl, aryl or halogen, nuclear or side chain derivatives, for example 4-chlorstyrene, 4-chlor-b -chlorstyrene, 4 - brom - b - methylstyrene, 4 - ethylstyrene, 2-, 3- and 4-methylstyrenes, and a -methylstyrene. For phenyl methyl carbinol, pressure is preferably below 100, especially 30-70 mm., and temperature above 300 DEG , especially 350-450 DEG C. Preferred conditions are about 50 mm. and 380-420 DEG C. Activated alumina, especially in massive form, for example as pellets, is the preferred catalyst. Others include other metal oxides, and phosphoric acid or a phosphate on a carrier. Catalytic activity is restored as required by heating to 400-450 DEG C. in air. Hydroquinone or other polymerization inhibitor, for example in an amount of 0.1 per cent by weight, may be mixed with the phenyl methyl carbinol. In one example, phenyl methyl carbinol, which may contain hydroquinone, is treated at 400 DEG C. and 50 mm. with activated alumina, the products condensed and stratified, and the upper layer distilled at 50 mm. in presence of hydroquinone. The 4-chlor derivative is similarly dehydrated at about 45 mm.
GB653545A 1945-03-15 1945-03-15 Improvements in the manufacture of styrene and derivatives of styrene Expired GB589015A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB653545A GB589015A (en) 1945-03-15 1945-03-15 Improvements in the manufacture of styrene and derivatives of styrene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB653545A GB589015A (en) 1945-03-15 1945-03-15 Improvements in the manufacture of styrene and derivatives of styrene

Publications (1)

Publication Number Publication Date
GB589015A true GB589015A (en) 1947-06-09

Family

ID=9816268

Family Applications (1)

Application Number Title Priority Date Filing Date
GB653545A Expired GB589015A (en) 1945-03-15 1945-03-15 Improvements in the manufacture of styrene and derivatives of styrene

Country Status (1)

Country Link
GB (1) GB589015A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2736948A1 (en) * 1977-08-17 1979-03-01 Dow Chemical Co Alpha-alkyl-benzyl alcohols dehydration - to form monovinylidene aromatic monomers using silica gel
US4233467A (en) * 1979-03-12 1980-11-11 The Dow Chemical Company Dehydration of α-methylbenzyl alcohols to form monovinylidene aromatic monomers
US4273622A (en) 1978-06-22 1981-06-16 Halcon Research & Development Corp. Method of treating alpha-methylbenzylalcohol dehydration products

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2736948A1 (en) * 1977-08-17 1979-03-01 Dow Chemical Co Alpha-alkyl-benzyl alcohols dehydration - to form monovinylidene aromatic monomers using silica gel
US4273622A (en) 1978-06-22 1981-06-16 Halcon Research & Development Corp. Method of treating alpha-methylbenzylalcohol dehydration products
US4233467A (en) * 1979-03-12 1980-11-11 The Dow Chemical Company Dehydration of α-methylbenzyl alcohols to form monovinylidene aromatic monomers

Similar Documents

Publication Publication Date Title
GB1182068A (en) Process for the Production of Metal Acetylacetonates
GB589015A (en) Improvements in the manufacture of styrene and derivatives of styrene
GB1398377A (en) Preparation of resorcinol and alkyl-substituted derivatives thereof
GB933149A (en) Production of conjugated diolefines
GB765468A (en) Improvements in and relating to the production of alumina/silica catalysts
Effenberger et al. New aspects of the Fries rearrangement
GB1023167A (en) Process for the production of malonic acid dinitrile from cyanacetamide
GB942944A (en) Dehydrogenation of aliphatic hydrocarbons and catalyst therefor
GB1009555A (en) Production of xylene
GB778014A (en) A process for alkylating benzene or a mono-alkyl benzene or a mixture thereof in the liquid phase
GB621812A (en) Process for dehydrating castor oil
GB783761A (en) Process for the production of alcohols
SU148797A1 (en) The method of obtaining mono - and dialkylbenzenes
JPS5236629A (en) Process for preparation of p- diisopropenylbenzene
SU603212A1 (en) WAY OF OBTAINING 4-METHYL-5,6-DIHYDROPYRANA
JPS5545664A (en) Production of styrene by dehydration of alpha-phenylethyl alcohol
GB961668A (en) Process for the manufacture of acrylonitrile
GB790994A (en) Production of pyridine bases
GB939214A (en) Methods of preparing cracking catalyst and use thereof
FR1171021A (en) Process for the preparation of condensation products suitable as adjuvants for textiles
GB788349A (en) Process for the synthesis of 1-bromo-4-chlorobutane
FR2134808A5 (en) Insecticidal ddvp compsns - stabilised with styrenes and derivs to give prolonged activity
GB608538A (en) Conversion products of 2:3-dihydropyran
GB361153A (en) Improvements in or relating to the manufacture of acrylic acid esters
BE595439A (en) Process for the preparation of aromatic condensation products.