GB267940A - Manufacture of condensation products from aromatic hydrocarbons or derivatives thereof - Google Patents

Manufacture of condensation products from aromatic hydrocarbons or derivatives thereof

Info

Publication number
GB267940A
GB267940A GB7322/27A GB732227A GB267940A GB 267940 A GB267940 A GB 267940A GB 7322/27 A GB7322/27 A GB 7322/27A GB 732227 A GB732227 A GB 732227A GB 267940 A GB267940 A GB 267940A
Authority
GB
United Kingdom
Prior art keywords
methyl
sulphuric acid
chloride
acid
aromatic hydrocarbons
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
GB7322/27A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB267940A publication Critical patent/GB267940A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/76Ketones containing a keto group bound to a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/02Ortho- or ortho- and peri-condensed systems
    • C07C2603/04Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2603/06Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
    • C07C2603/10Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
    • C07C2603/12Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
    • C07C2603/16Benz[e]indenes; Hydrogenated benz[e]indenes

Landscapes

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

Abstract

267,940. I. G. Farbenindustrie Akt.- Ges. March 16, 1926, [Convention date]. Samples furnished. Indanones are obtained by treating aromatic hydrocarbons and their substitution products with a halide of a #-halogen-substituted fatty acid, converting the halogenated ketone thus obtained into an unsaturated ketone by means of an agent capable of splitting off hydrogen halide. e.g. by distillation or bv the action of sulphuric acid, and finally treating the unsaturated ketone with an acid condensing agent, e.g. aluminium chloride or sulphuric acid. The reaction may be conducted in several stages or in a single operation. In examples (1) 1-methylnaphthalene is treated with #-chlorpropionyl chloride in the presence of a suspension of aluminium chloride in carbon disulphide, the 1-methyl-4-#-chlorpropionyl-naphthalene obtained is heated with sulphuric acid and the product is poured into water; 5-methyl- 6: 7-benzo-1-indanone separates out and (2) 1- methylnaphthalene is similarly treated with #- chlorbutyryl chloride to yield 1-methyl-4-#- chlorbutyryl-naphthalene, this is distilled in a vacuum to form 1-methyl-4-crotonylnaphthalene which yields 3 : 5-dimethyl-6 : 7-benzo-1-indanone when heated with sulphuric acid. The Specification as open to inspection under Sect. 91 (3) (a) comprises also the use of substitution products of halides of #-halogen-substituted fatty acids as parent materials. This subjectmatter does not appear in the Specification as accepted.
GB7322/27A 1926-03-16 1927-03-16 Manufacture of condensation products from aromatic hydrocarbons or derivatives thereof Expired GB267940A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE267940X 1926-03-16

Publications (1)

Publication Number Publication Date
GB267940A true GB267940A (en) 1928-06-14

Family

ID=5997655

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7322/27A Expired GB267940A (en) 1926-03-16 1927-03-16 Manufacture of condensation products from aromatic hydrocarbons or derivatives thereof

Country Status (1)

Country Link
GB (1) GB267940A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3950408A (en) * 1974-02-15 1976-04-13 Merck & Co., Inc. Process for preparing [1-oxo-2-cyclopentyl (or 2-isopropyl)-2-methyl-6,7-dichloro-5-indanyloxy] acetic acid

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3950408A (en) * 1974-02-15 1976-04-13 Merck & Co., Inc. Process for preparing [1-oxo-2-cyclopentyl (or 2-isopropyl)-2-methyl-6,7-dichloro-5-indanyloxy] acetic acid

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