GB739907A - Recovery of phenols - Google Patents

Recovery of phenols

Info

Publication number
GB739907A
GB739907A GB22677/52A GB2267752A GB739907A GB 739907 A GB739907 A GB 739907A GB 22677/52 A GB22677/52 A GB 22677/52A GB 2267752 A GB2267752 A GB 2267752A GB 739907 A GB739907 A GB 739907A
Authority
GB
United Kingdom
Prior art keywords
resorcinol
meta
isopropenylphenol
heat treatment
inert diluent
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
GB22677/52A
Inventor
David Ian Hutchinson Jacobs
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.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co Ltd
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 Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB22677/52A priority Critical patent/GB739907A/en
Publication of GB739907A publication Critical patent/GB739907A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/68Purification; separation; Use of additives, e.g. for stabilisation
    • C07C37/86Purification; separation; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification

Landscapes

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

Abstract

A process for the production of resorcinol by the catalytic cleavage of a reaction mixture containing meta-di-isopropylbenzene hydroperoxide derived from the oxidation of meta-di-isopropylbenzene comprises decomposing by the action of heat the material contained in the cleavage reaction product which is less volatile than resorcinol and recovering the additional quantities of resorcinol and the meta-isopropenylphenol so formed. The heat treatment may be conducted in presence of an acid catalyst or, alternatively, the cleavage reaction product is treated to remove or neutralize cleavage catalysts and stripped of low-boiling materials before being subjected to heat treatment. The heat treatment is also preferably conducted at 200-400 DEG C. at super- or sub-atmospheric pressures and in presence of a high-boiling inert diluent (preferably boiling at or above 200 DEG C., e.g. tri-isopropyl- or 1 : 2 : 4-trichlorobenzene; isopropyl-, methyl-, chloro- or bromonaphthalene; a gas oil fraction; or a mixture thereof), the heat-treated cleavage reaction product being distilled and the resorcinol and meta-isopropenylphenol recovered from the distillate preferably by crystallization and filtration, or by distilling directly into water. The heat treatment and distillation are preferably conducted simultaneously, and the proportion of high-boiling inert diluent is preferably adjusted so that the distillate is not saturated with respect to resorcinol while still above the temperature at which crystallization takes place. Further quantities of resorcinol may be recovered from solution in the inert diluent mother-liquors by extraction with water; meta-isopropenylphenol is also recovered by extracting the resorcinol-free inert diluent with an aqueous alkaline solution. Mixed resorcinol/meta-isopropenylphenol phases are separated (1) by extraction with a solvent, e.g. benzene, toluene, methyl-naphthalene, chloroform or carbon tetrachloride; or (2) by partition between two immiscible solvents, e.g. water and one of the solvents in (1). The resorcinol, after separation from the meta-isopropenyl phenol, may be further purified by redistillation, or by sublimation.
GB22677/52A 1952-09-10 1952-09-10 Recovery of phenols Expired GB739907A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB22677/52A GB739907A (en) 1952-09-10 1952-09-10 Recovery of phenols

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB22677/52A GB739907A (en) 1952-09-10 1952-09-10 Recovery of phenols

Publications (1)

Publication Number Publication Date
GB739907A true GB739907A (en) 1955-11-02

Family

ID=10183322

Family Applications (1)

Application Number Title Priority Date Filing Date
GB22677/52A Expired GB739907A (en) 1952-09-10 1952-09-10 Recovery of phenols

Country Status (1)

Country Link
GB (1) GB739907A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2404615A1 (en) * 1977-09-30 1979-04-27 Mitsui Petrochemical Ind RECOVERY AND RESORCINOL PROCESS
US4239921A (en) * 1978-07-10 1980-12-16 Mitsu, Petrochemical Industries, Ltd. Process for purification of crude resorcinol
US4283567A (en) * 1978-12-20 1981-08-11 Mitsui Petrochemical Industries Ltd. Method for recovering resorcinol
EP0280403A1 (en) * 1987-02-09 1988-08-31 Hoechst Celanese Corporation Process for dearylation of alkylenebisphenols and alkyltrisphenols
WO1991005755A1 (en) * 1989-10-17 1991-05-02 Owafin Ag Process for manufacturing bisphenols
CN115636913A (en) * 2022-09-27 2023-01-24 山东阳谷华泰化工股份有限公司 Preparation method of low-free-phenol phenolic resin

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2404615A1 (en) * 1977-09-30 1979-04-27 Mitsui Petrochemical Ind RECOVERY AND RESORCINOL PROCESS
US4192958A (en) * 1977-09-30 1980-03-11 Mitsui Petrochemical Industries Ltd. Method for recovering resorcinol
US4239921A (en) * 1978-07-10 1980-12-16 Mitsu, Petrochemical Industries, Ltd. Process for purification of crude resorcinol
US4283567A (en) * 1978-12-20 1981-08-11 Mitsui Petrochemical Industries Ltd. Method for recovering resorcinol
EP0280403A1 (en) * 1987-02-09 1988-08-31 Hoechst Celanese Corporation Process for dearylation of alkylenebisphenols and alkyltrisphenols
WO1991005755A1 (en) * 1989-10-17 1991-05-02 Owafin Ag Process for manufacturing bisphenols
CN115636913A (en) * 2022-09-27 2023-01-24 山东阳谷华泰化工股份有限公司 Preparation method of low-free-phenol phenolic resin

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