GB1431640A - Process for the preparation of aliphatically unsaturated aromati amino compounds - Google Patents

Process for the preparation of aliphatically unsaturated aromati amino compounds

Info

Publication number
GB1431640A
GB1431640A GB5440874A GB5440874A GB1431640A GB 1431640 A GB1431640 A GB 1431640A GB 5440874 A GB5440874 A GB 5440874A GB 5440874 A GB5440874 A GB 5440874A GB 1431640 A GB1431640 A GB 1431640A
Authority
GB
United Kingdom
Prior art keywords
group
nitro
ring
aromatic
amino
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
GB5440874A
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.)
Bayer AG
Original Assignee
Bayer 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
Priority claimed from DE2362780A external-priority patent/DE2362780C3/en
Priority claimed from DE2425811A external-priority patent/DE2425811C3/en
Application filed by Bayer AG filed Critical Bayer AG
Publication of GB1431640A publication Critical patent/GB1431640A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44—Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
    • B01J27/04—Sulfides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
    • B01J27/04—Sulfides
    • B01J27/043—Sulfides with iron group metals or platinum group metals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/30—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds
    • C07C209/32—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds by reduction of nitro groups
    • C07C209/36—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of nitrogen-to-oxygen or nitrogen-to-nitrogen bonds by reduction of nitro groups by reduction of nitro groups bound to carbon atoms of six-membered aromatic rings in presence of hydrogen-containing gases and a catalyst
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/58—[b]- or [c]-condensed
    • C07D209/72—4,7-Endo-alkylene-iso-indoles
    • C07D209/76—4,7-Endo-alkylene-iso-indoles with oxygen atoms in positions 1 and 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
    • C07D249/18—Benzotriazoles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Indole Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

1431640 Aliphatically unsaturated aromatic amino compounds BAYER AG 17 Dec 1974 [18 Dec 1973 28 May 1974] 54408/74 Heading C2C [Also in Division C1] Aromatic amines wherein the amino group is aromatically bonded and which contain aliphatic C-C multiple bonds are obtained by hydrogenation of aromatic nitro compounds wherein the nitro group is aromatically bonded and which contain aliphatic C-C multiple bonds in the presence of metal sulphides of the formula wherein M is a metal of Group VIII of the Periodic Table or rhenium, and x is 1 to 4, as catalyst, at 20‹ to 140‹ C. and 5 to 150 bars H 2 pressure. The hydrogenation may be carried out in an inert solvent. In nitro compounds to be used as starting materials in this process there may be more than one nitro group and one or more olefinic bonds present; the olefinic bond may occur as an isolated bond in a carbon chain, in or attached to a cycloaliphatic ring, in or attached to a heterocyclic ring or attached to an aromatic ring, and may be in conjugation with a carbonyl, carboxyl, CN, SO 2 or phosphorus group. The group containing the olefinic bond can be bonded directly to the aromatic ring which bears the nitro group, or can be bonded via a -SO 2 -, -O-, -S-, -CO-, -CONH-, -COO-, amino, imino, imide, imino-imide, phenyl or heterocyclic group, and the heterocyclic group or the phenyl group may be fused to the ring which bears the nitro group.
GB5440874A 1973-12-18 1974-12-17 Process for the preparation of aliphatically unsaturated aromati amino compounds Expired GB1431640A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2362780A DE2362780C3 (en) 1973-12-18 1973-12-18 Process for the preparation of unsaturated amino compounds
DE2425811A DE2425811C3 (en) 1974-05-28 1974-05-28 Process for the preparation of unsaturated aromatic amino compounds

Publications (1)

Publication Number Publication Date
GB1431640A true GB1431640A (en) 1976-04-14

Family

ID=25766257

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5440874A Expired GB1431640A (en) 1973-12-18 1974-12-17 Process for the preparation of aliphatically unsaturated aromati amino compounds

Country Status (8)

Country Link
JP (1) JPS5093927A (en)
BR (1) BR7410570D0 (en)
CH (1) CH598189A5 (en)
DD (1) DD118415A5 (en)
ES (1) ES432989A1 (en)
FR (1) FR2254553B1 (en)
GB (1) GB1431640A (en)
NL (1) NL7416449A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4215226A (en) * 1978-11-06 1980-07-29 Gulf Research & Development Company Selective hydrogenation of nitroaromatic acetylenes over an unsupported RuS2 catalyst
US4216341A (en) * 1978-11-06 1980-08-05 Gulf Research & Development Company Selective hydrogenation of certain nitroaromatic hydroxy substituted acetylenes over a heterogeneous RuS2 catalyst
US4219679A (en) * 1978-11-06 1980-08-26 Gulf Research & Development Company Selective hydrogenation of nitro groups on nitroaromatic acetylenes using an unsupported cobalt polysulfide catalyst

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1331876C (en) * 1987-10-02 1994-09-06 Exxon Research And Engineering Company High surface area rhenium sulfide hydrodesulfurization catalysts prepared by an aqueous technique and a process for using them

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4215226A (en) * 1978-11-06 1980-07-29 Gulf Research & Development Company Selective hydrogenation of nitroaromatic acetylenes over an unsupported RuS2 catalyst
US4216341A (en) * 1978-11-06 1980-08-05 Gulf Research & Development Company Selective hydrogenation of certain nitroaromatic hydroxy substituted acetylenes over a heterogeneous RuS2 catalyst
US4219679A (en) * 1978-11-06 1980-08-26 Gulf Research & Development Company Selective hydrogenation of nitro groups on nitroaromatic acetylenes using an unsupported cobalt polysulfide catalyst

Also Published As

Publication number Publication date
ES432989A1 (en) 1977-02-16
NL7416449A (en) 1975-06-20
FR2254553A1 (en) 1975-07-11
FR2254553B1 (en) 1978-07-07
CH598189A5 (en) 1978-04-28
JPS5093927A (en) 1975-07-26
DD118415A5 (en) 1976-03-05
BR7410570D0 (en) 1975-09-02

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee