JPS55133333A - Selective separation of 2,6-dinitrotoluene from dinitrotoluene mixture - Google Patents
Selective separation of 2,6-dinitrotoluene from dinitrotoluene mixtureInfo
- Publication number
- JPS55133333A JPS55133333A JP4123779A JP4123779A JPS55133333A JP S55133333 A JPS55133333 A JP S55133333A JP 4123779 A JP4123779 A JP 4123779A JP 4123779 A JP4123779 A JP 4123779A JP S55133333 A JPS55133333 A JP S55133333A
- Authority
- JP
- Japan
- Prior art keywords
- species
- dinitrotoluene
- mixture
- title compound
- under pressure
- 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.)
- Pending
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
PURPOSE: To obtain the title compound which is useful as an intermediate for syntheses of perfumes, medicines, etc. safely in high purity, by the selective reduction of 2,4-species through the hydrogenation of dinitrotoluene mixture in the presence of a catalyst under pressure.
CONSTITUTION: Mixture of 2,4- and 2,6-dinitrotoluenes is hydrogenated in an autoclave under pressure, preferably at 40W50atm, in the presence of a catalyst such as palladium carbon, Raney mickel, Raney cobalt or platinum black, preferably at 40W50°C. Thereby, nitro group at 4 position of the 2,4-species recieves reductive action most easily, and the 2,4-species is selectively converted into an amine by the addition of hydrogen in an amount corresponding to 4 position of the 2,4-species. The title compound is obtained by removing the amine part from a reaction mixture through acid treatment and recrystallizing the residual non-amine part. Methyl alcohol, benzene, dimethylformamide, etc. is preferably used as a solvent in said reaction.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4123779A JPS55133333A (en) | 1979-04-04 | 1979-04-04 | Selective separation of 2,6-dinitrotoluene from dinitrotoluene mixture |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4123779A JPS55133333A (en) | 1979-04-04 | 1979-04-04 | Selective separation of 2,6-dinitrotoluene from dinitrotoluene mixture |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS55133333A true JPS55133333A (en) | 1980-10-17 |
Family
ID=12602807
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4123779A Pending JPS55133333A (en) | 1979-04-04 | 1979-04-04 | Selective separation of 2,6-dinitrotoluene from dinitrotoluene mixture |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS55133333A (en) |
-
1979
- 1979-04-04 JP JP4123779A patent/JPS55133333A/en active Pending
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