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GB947308A - Improvements in or relating to nuclear-chlorinated aromatic compounds - Google Patents

Improvements in or relating to nuclear-chlorinated aromatic compounds

Info

Publication number
GB947308A
GB947308A GB1477460A GB1477460A GB947308A GB 947308 A GB947308 A GB 947308A GB 1477460 A GB1477460 A GB 1477460A GB 1477460 A GB1477460 A GB 1477460A GB 947308 A GB947308 A GB 947308A
Authority
GB
United Kingdom
Prior art keywords
mixture
chloride
benzoic acids
benzotrichlorides
dichlorobenzaldehyde
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
GB1477460A
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.)
Koninklijke Philips NV
Original Assignee
Philips Gloeilampenfabrieken NV
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 Philips Gloeilampenfabrieken NV filed Critical Philips Gloeilampenfabrieken NV
Publication of GB947308A publication Critical patent/GB947308A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/42Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrolysis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/093Preparation of halogenated hydrocarbons by replacement by halogens
    • C07C17/10Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
    • C07C17/14Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms in the side-chain of aromatic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C25/00Compounds containing at least one halogen atom bound to a six-membered aromatic ring
    • C07C25/02Monocyclic aromatic halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/42Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrolysis
    • C07C45/43Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrolysis of >CX2 groups, X being halogen

Landscapes

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

Abstract

A mixture of isomeric dichlorotoluenes including the 2,6-isomer is chlorinated in the presence of light and in the absence of a nuclear halogenation catalyst to produce a mixture of 2,6-dichlorobenzal chloride and dichlorobenzo-trichlorides and the 2,6-dichlorobenzal chloride is separated from the mixture. This separation may be effected by treating the mixture with steam, hot water of dilute mineral acid to hydrolyse the benzotrichlorides to the corresponding benzoic acids, making the hydrolysate alkaline to bring the benzoic acids into solution as soluble salts and 1 separating the isoluble dichlorobenzal chloride from the solution. The benzal chloride may be hydrolysed, preferably with 93% by weight sulphuric acid, to 2,6-dichlorobenzaldehyde either before or after separation from the benzotrichlorides. In the former case both components are hydrolysed and the benzaldehyde may be separated from the benzoic acids by converting the latter into water soluble salts. Examples are given. Specification 862,863 is referred to.ALSO:A fungicidal composition comprises 2,6-dichlorobenzaldehyde mixed with a solid or liquid inert carrier, with or without one or more other additives comprising surface-active agents, dispersion agents and adhesives.
GB1477460A 1959-04-28 1960-04-27 Improvements in or relating to nuclear-chlorinated aromatic compounds Expired GB947308A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL238690 1959-04-28

Publications (1)

Publication Number Publication Date
GB947308A true GB947308A (en) 1964-01-22

Family

ID=19751696

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1477460A Expired GB947308A (en) 1959-04-28 1960-04-27 Improvements in or relating to nuclear-chlorinated aromatic compounds

Country Status (4)

Country Link
BE (1) BE590257A (en)
CH (1) CH404624A (en)
GB (1) GB947308A (en)
NL (1) NL238690A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115433069A (en) * 2022-08-23 2022-12-06 柳州东风容泰化工股份有限公司 Preparation method of 2, 4-dichlorobenzaldehyde

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115433069A (en) * 2022-08-23 2022-12-06 柳州东风容泰化工股份有限公司 Preparation method of 2, 4-dichlorobenzaldehyde

Also Published As

Publication number Publication date
CH404624A (en) 1965-12-31
NL238690A (en)
BE590257A (en)

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