GB250819A - Manufacture of diarylamines - Google Patents

Manufacture of diarylamines

Info

Publication number
GB250819A
GB250819A GB2274925A GB2274925A GB250819A GB 250819 A GB250819 A GB 250819A GB 2274925 A GB2274925 A GB 2274925A GB 2274925 A GB2274925 A GB 2274925A GB 250819 A GB250819 A GB 250819A
Authority
GB
United Kingdom
Prior art keywords
toluidine
ditolylamine
nuclear
chlortoluene
catalyst
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
GB2274925A
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.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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 Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Priority to GB2274925A priority Critical patent/GB250819A/en
Publication of GB250819A publication Critical patent/GB250819A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

250,819. Imray, O. Y., (Soc. of Chemical Industry in Basle). Sept. 11, 1925. Nuclear substitution products of diphenylamine are prepared by causing a nuclear halogen substitution product of a benzene hydrocarbon to act on an alkali-metal compound of a primary aromatic amino-body of the benzene series, if desired in presence of a catalyst, either one or both of the reacting substances containing at least one nuclear substituent in addition to the halogen atom or amino group. In an example, o-o<1>-ditolylamine is obtained by heating o-toluidine with sodium and o-chlortoluene in the presence of copper powder as a catalyst. In a similar manner, o-tolylphenylamine may be obtained from ochlortoluene and aniline or from o-toluidine and brombenzene, o-p-ditolylamine from p-chlortoluene and o-toluidine, and 4<1>-chlor-o-o<1>-ditolylamine from 2: 5-dichlortoluene and o-toluidine.
GB2274925A 1925-09-11 1925-09-11 Manufacture of diarylamines Expired GB250819A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2274925A GB250819A (en) 1925-09-11 1925-09-11 Manufacture of diarylamines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2274925A GB250819A (en) 1925-09-11 1925-09-11 Manufacture of diarylamines

Publications (1)

Publication Number Publication Date
GB250819A true GB250819A (en) 1926-04-22

Family

ID=10184460

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2274925A Expired GB250819A (en) 1925-09-11 1925-09-11 Manufacture of diarylamines

Country Status (1)

Country Link
GB (1) GB250819A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3155727A (en) * 1960-07-25 1964-11-03 Goodyear Tire & Rubber Reaction of aromatic amines with para halo nitrobenzenes using copper cyanide condensation catalyst

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3155727A (en) * 1960-07-25 1964-11-03 Goodyear Tire & Rubber Reaction of aromatic amines with para halo nitrobenzenes using copper cyanide condensation catalyst

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