GB1507320A - Manufacture of dimethylaminobenzene compounds - Google Patents

Manufacture of dimethylaminobenzene compounds

Info

Publication number
GB1507320A
GB1507320A GB3314175A GB3314175A GB1507320A GB 1507320 A GB1507320 A GB 1507320A GB 3314175 A GB3314175 A GB 3314175A GB 3314175 A GB3314175 A GB 3314175A GB 1507320 A GB1507320 A GB 1507320A
Authority
GB
United Kingdom
Prior art keywords
manufacture
optionally substituted
substituted aliphatic
hydrocarbon radical
radical
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
GB3314175A
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 SE
Original Assignee
BASF SE
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
Priority claimed from DE2438506A external-priority patent/DE2438506A1/en
Priority claimed from DE19742454405 external-priority patent/DE2454405A1/en
Application filed by BASF SE filed Critical BASF SE
Publication of GB1507320A publication Critical patent/GB1507320A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/52Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
    • C07D263/54Benzoxazoles; Hydrogenated benzoxazoles
    • C07D263/56Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/52Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
    • C07D263/54Benzoxazoles; Hydrogenated benzoxazoles
    • C07D263/58Benzoxazoles; Hydrogenated benzoxazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Indole Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

1507320 Manufacture of dimethylaminobenzenes BASF AG 8 Aug 1975 [10 Aug 1974 16 Nov 1974] 33141/75 Addition to 1462258 Heading C2C The invention comprises a process for the manufacture of compounds of Formula I wherein individual radicals R<SP>1</SP>, R<SP>2</SP>, R<SP>3</SP> are independently halogen, optionally substituted aliphatic or aromatic hydrocarbon radical -SO 3 R<SP>4</SP>, SO 2 N(R<SP>4</SP>) 2 , SO 2 R<SP>4</SP>, SO 2 NHCOR<SP>4</SP>, OR<SP>4</SP>, COR<SP>4</SP>, NHCOR<SP>4</SP> wherein R<SP>4</SP> is an optionally substituted aliphatic hydrocarbon radical, and the individual radicals R<SP>2</SP> and R<SP>3</SP> may also be independently hydrogen, phenoxy or -CO 2 R<SP>5</SP>, R<SP>5</SP> being an optionally substituted aliphatic, cycloaliphatic, araliphatic or aromatic hydrocarbon radical, and adjacent radicals R<SP>3</SP> or R<SP>1</SP> and an adjacent radical R<SP>3</SP> may also, together with the two carbon atoms linking them, form a fused heterocyclic radical, wherein a nitrobenzene of Formula II in which R<SP>1</SP>, R<SP>2</SP>, and R<SP>3</SP> are as defined above is reacted with formaldehyde and hydrogen in the presence of a hydrogenation catalyst containing one or more metals of atomic number 24 to 29 and of a weak organic acid at 35‹ to 150‹ C. and a pressure of at least 40 atmospheres.
GB3314175A 1974-08-10 1975-08-08 Manufacture of dimethylaminobenzene compounds Expired GB1507320A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2438506A DE2438506A1 (en) 1974-08-10 1974-08-10 Nuclear substd. N,N-dimethyl-anilines prepn. - by reacting substd. nitrobenzenes with formaldehyde under reducing conditions
DE19742454405 DE2454405A1 (en) 1974-11-16 1974-11-16 Dimethyl amino benzene derivs prepn - inters for dyes and pesticides, photoinitiators, resin stabilisers and anti oedemics

Publications (1)

Publication Number Publication Date
GB1507320A true GB1507320A (en) 1978-04-12

Family

ID=25767537

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3314175A Expired GB1507320A (en) 1974-08-10 1975-08-08 Manufacture of dimethylaminobenzene compounds

Country Status (4)

Country Link
JP (1) JPS51125028A (en)
FR (1) FR2281341A2 (en)
GB (1) GB1507320A (en)
IT (1) IT1049559B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5135944B2 (en) * 2007-08-09 2013-02-06 東ソー株式会社 Process for producing N, N-dimethylcyclohexylamine

Also Published As

Publication number Publication date
FR2281341A2 (en) 1976-03-05
FR2281341B2 (en) 1979-09-21
JPS51125028A (en) 1976-11-01
IT1049559B (en) 1981-02-10

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Legal Events

Date Code Title Description
PS Patent sealed