DE108165C - - Google Patents
Info
- Publication number
- DE108165C DE108165C DENDAT108165D DE108165DA DE108165C DE 108165 C DE108165 C DE 108165C DE NDAT108165 D DENDAT108165 D DE NDAT108165D DE 108165D A DE108165D A DE 108165DA DE 108165 C DE108165 C DE 108165C
- Authority
- DE
- Germany
- Prior art keywords
- chlorine
- dinitrobenzene
- carrier
- dinitrochlorobenzene
- symmetrical
- 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
Links
- 239000000460 chlorine Substances 0.000 claims description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- WDCYWAQPCXBPJA-UHFFFAOYSA-N 1,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1 WDCYWAQPCXBPJA-UHFFFAOYSA-N 0.000 claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- VYZAHLCBVHPDDF-UHFFFAOYSA-N Dinitrochlorobenzene Chemical compound [O-][N+](=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 VYZAHLCBVHPDDF-UHFFFAOYSA-N 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- FAPDDOBMIUGHIN-UHFFFAOYSA-K antimony trichloride Chemical compound Cl[Sb](Cl)Cl FAPDDOBMIUGHIN-UHFFFAOYSA-K 0.000 claims 1
- 238000001816 cooling Methods 0.000 claims 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 238000001953 recrystallisation Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000005660 chlorination reaction Methods 0.000 description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- KMAQZIILEGKYQZ-UHFFFAOYSA-N 1-chloro-3-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(Cl)=C1 KMAQZIILEGKYQZ-UHFFFAOYSA-N 0.000 description 1
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical group CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001804 chlorine Chemical class 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE108165C true DE108165C (enrdf_load_stackoverflow) | 1900-01-01 |
Family
ID=378160
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT108165D Expired DE108165C (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE108165C (enrdf_load_stackoverflow) |
-
0
- DE DENDAT108165D patent/DE108165C/de not_active Expired
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE108165C (enrdf_load_stackoverflow) | ||
DE1543969A1 (de) | Neue Guanidinderivate,ihre Herstellung und Verwendung | |
DE91150C (de) | Verfahren zur einführung von aminresten in oxyanthrachinone | |
DE901888C (de) | Verfahren zur Herstellung von fungiziden, Chlor und Stickstoff enthaltenden Derivaten des Cyclohexadienons | |
DE1206422B (de) | Verfahren zur Herstellung von 2, 6-Dichlorbenzonitril | |
DE1645890A1 (de) | Verfahren zur Herstellung substituierter epsilon-Caprolactame | |
DE228901C (enrdf_load_stackoverflow) | ||
DE742257C (de) | Verfahren zur Herstellung von N-Aryl-3-oxypyrrolidinen | |
DE134306C (enrdf_load_stackoverflow) | ||
DE959095C (de) | Verfahren zur Herstellung von Pyridazonderivaten | |
DE3316227A1 (de) | Verfahren zur herstellung von hexafluoroisobuten und/oder hexafluorobuten | |
DE1643621C3 (enrdf_load_stackoverflow) | ||
DE216715C (enrdf_load_stackoverflow) | ||
DE1163803B (de) | Verfahren zur Herstellung von 3-Aryl-1,1,3,3-tetrachlor-2-aza-propenen | |
DE1670706C3 (de) | Verfahren zur Herstellung substituierter 2-ChIorbenzothiazole | |
DE102068C (enrdf_load_stackoverflow) | ||
DE495337C (de) | Verfahren zur Darstellung organischer Basen | |
DE125094C (enrdf_load_stackoverflow) | ||
DE1670802C (de) | Verfahren zur Herstellung von Indoldenvaten | |
DE1793731C3 (de) | 5-Chlor-2-(hydroxyamino-acetamino)benzophenon | |
DE206537C (enrdf_load_stackoverflow) | ||
DE277396C (enrdf_load_stackoverflow) | ||
DE419814C (de) | Verfahren zur Darstellung von hochchlorierten stickstoffhaltigen hydroaromatischen Produkten | |
DE1300546B (de) | N-Methylcarbaminsaeure-(4-benzylidenamino)-phenylester | |
DE3737497A1 (de) | Verfahren zur herstellung von 6-chlorisatosaeureanhydrid |