GEP19991744B - Process for Preparing Substituted Aromatic Amines, Process for Preparing 4-aminodiphenylamin (4-adpa), Process for Preparing Alkylated Aromatic Amines - Google Patents
Process for Preparing Substituted Aromatic Amines, Process for Preparing 4-aminodiphenylamin (4-adpa), Process for Preparing Alkylated Aromatic AminesInfo
- Publication number
- GEP19991744B GEP19991744B GEAP19942928A GEAP1994002928A GEP19991744B GE P19991744 B GEP19991744 B GE P19991744B GE AP19942928 A GEAP19942928 A GE AP19942928A GE AP1994002928 A GEAP1994002928 A GE AP1994002928A GE P19991744 B GEP19991744 B GE P19991744B
- Authority
- GE
- Georgia
- Prior art keywords
- preparing
- aromatic amines
- protic material
- base
- product
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/54—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to two or three six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/02—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of hydrogen atoms by amino groups
-
- 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
- C07C209/42—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 nitrogen-to-nitrogen bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C245/00—Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
- C07C245/02—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides
- C07C245/06—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings
- C07C245/08—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings with the two nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings, e.g. azobenzene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1. Technical Result Simplification of technological process, increase in quality and yield of the final product. 2. Essence Substituted aromatic amines are prepared by contacting a nucleophylic compound which is selected from the group containing aniline, substituted derivatives thereof, aliphatic amine derivatives and amide with azo containing compound in the presence of a suitable base and protic material at a temperature of about 10°C to 150°C wherein the molar ratio of protic material to base is 0:1 to 5:1 and reducing the product of the contact to produce the final product. 4-aminodiphenylamin is produced by con¬tacting aniline and azobenzene in the presence of suitable base and protic material at temperature of about 10°C to 150°C at molar ratio of protic material to base 0:1 to 5:1 and reducing the product of the contact to produce the final product. Alkylated aromatic amines are produced by contacting a nucleophilic compounds which is selected from the group comprising aniline, substitute aliphatic amine derivative, aliphatic amin, aliphatic amin derivative and amide with nitrogen containing compound in the presence of suitable base and protic material at temperature of about 10°C to 150°C, at molar ratio of protic material to base being 0:1 to 5:1 is conducted alkylation by reducing the contact product and obtaining the final product. 3. Field of Application Organic chemistry. 3 ind. and 72 dep.cl., 1 tabl.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/051,964 US5451702A (en) | 1993-04-26 | 1993-04-26 | Process for preparing substituted aromatic amines |
Publications (1)
Publication Number | Publication Date |
---|---|
GEP19991744B true GEP19991744B (en) | 1999-09-10 |
Family
ID=66646904
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GEAP19942928A GEP19991744B (en) | 1993-04-26 | 1994-03-18 | Process for Preparing Substituted Aromatic Amines, Process for Preparing 4-aminodiphenylamin (4-adpa), Process for Preparing Alkylated Aromatic Amines |
Country Status (3)
Country | Link |
---|---|
KR (1) | KR0182064B1 (en) |
GE (1) | GEP19991744B (en) |
UA (1) | UA40682C2 (en) |
-
1994
- 1994-03-18 GE GEAP19942928A patent/GEP19991744B/en unknown
- 1994-03-18 KR KR1019950704426A patent/KR0182064B1/en not_active IP Right Cessation
- 1994-03-18 UA UA95104706A patent/UA40682C2/en unknown
Also Published As
Publication number | Publication date |
---|---|
KR960701825A (en) | 1996-03-28 |
KR0182064B1 (en) | 1999-05-15 |
UA40682C2 (en) | 2001-08-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GEP19991703B (en) | Method for Preparing Substituted Aromatic Amines | |
HU9503050D0 (en) | Process for preparing substituted aromatic amines | |
MD842G2 (en) | Method of preparing of 4-aminodiphenylamine | |
ES461680A1 (en) | Preparation of polyurethane ureas using as hardeners mixtures of water, amines, aldimines and ketimines | |
KR940001771B1 (en) | Process for the production of 2,2,6,6-tetraalkyl-4-piperidylamines | |
EP0343486A3 (en) | Process for the manufacture of n-(polyoxyalkyl)-n-(alkyl)amines | |
ATE158274T1 (en) | PROCESS FOR PRODUCING P-NITROAROMATIC AMINES AND PRODUCTS MADE THEREOF | |
TWI265919B (en) | Process for preparing 4-aminodiphenylamine intermediates | |
GEP19991744B (en) | Process for Preparing Substituted Aromatic Amines, Process for Preparing 4-aminodiphenylamin (4-adpa), Process for Preparing Alkylated Aromatic Amines | |
US4431841A (en) | Process for making diarylamines | |
PT90607A (en) | PREPARATION PROCESS OF AZACYLICCYLOBOXYL ACID DERIVATIVES | |
US4845297A (en) | Process for producing polyamines | |
US5262539A (en) | Process for the preparation of aromatic amines | |
CA1055048A (en) | Process for the cyanoethylation of aromatic amines | |
AU7324894A (en) | Process for preparing p-nitroaromatic amides and products thereof | |
HUP9700526A2 (en) | Process for reductive alkylation of polyamines | |
US5612483A (en) | Process for the preparation of nitro-substituted arylamines | |
Jones et al. | Inhibition of α-chymotrypsin by hydroxymethyl analogues of d-and lN-acetylphenylalanine and N-acetyltryptophan of potential affinity labeling value | |
CA1182467A (en) | Process for the preparation of n-monosubstituted o- alkylurethanes | |
EP0588060A3 (en) | Method for preparing aromatic secondary amino compound | |
Peters et al. | Process for Making Polyimides | |
JPS56115770A (en) | Preparation of indole or indole derivative | |
JPS6032780A (en) | Preparation of polyamine | |
RU97101086A (en) | IMPROVED METHOD FOR AMINATING PYRIDINE BASES UNDER CHICHIBIN | |
IL143172A0 (en) | A process for preparing a tertiary amine |