DE143449C - - Google Patents
Info
- Publication number
- DE143449C DE143449C DENDAT143449D DE143449DA DE143449C DE 143449 C DE143449 C DE 143449C DE NDAT143449 D DENDAT143449 D DE NDAT143449D DE 143449D A DE143449D A DE 143449DA DE 143449 C DE143449 C DE 143449C
- Authority
- DE
- Germany
- Prior art keywords
- chloro
- phenol
- nitro
- chlorophenol
- nitration
- 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.)
- Active
Links
- 238000006396 nitration reaction Methods 0.000 claims description 4
- 238000000034 method Methods 0.000 claims 1
- 239000000047 product Substances 0.000 description 5
- HORNXRXVQWOLPJ-UHFFFAOYSA-N 3-chlorophenol Chemical compound OC1=CC=CC(Cl)=C1 HORNXRXVQWOLPJ-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 2
- PNLPXABQLXSICH-UHFFFAOYSA-N 4-amino-3-chlorophenol Chemical compound NC1=CC=C(O)C=C1Cl PNLPXABQLXSICH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- CINHAXSZAFJRPW-UHFFFAOYSA-N 2-(chloroamino)phenol Chemical compound OC1=CC=CC=C1NCl CINHAXSZAFJRPW-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- QBGLHYQUZJDZOO-UHFFFAOYSA-N 2-chloro-3-nitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1Cl QBGLHYQUZJDZOO-UHFFFAOYSA-N 0.000 description 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/74—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
- C07C215/76—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton of the same non-condensed six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE143449C true DE143449C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Family
ID=410943
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT143449D Active DE143449C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE143449C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
-
0
- DE DENDAT143449D patent/DE143449C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2025662A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE143449C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE2501899C2 (de) | Verfahren zur herstellung von 2- nitro-4,6-dichlor-5-methylphenol | |
| DE2125095C3 (de) | Verfahren zur Abtrennung der Metallkomponenten aus einem wäßrigen Medium durch Flüssig/Flussig-Extraktion unter Verwendung eines Extraktionsmittels vom Hydroxyoxim-Typ | |
| DE2534210C3 (de) | Verfahren zur Seitenkettenchlorierung von perhalogenierten Methylaromaten und einige 4,4'-Bis-(cholormethyl)-ar-octahalogendiphenyläther | |
| DE228357C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE67018C (de) | Verfahren zur partiellen Reduction von Dinitroverbindungen | |
| DE2331892A1 (de) | Verfahren zur trennung von dialkylbenzoldihydroperoxiden | |
| DE69210245T2 (de) | N-Ethyl-Hydroxamsäure-Chelatbildner | |
| DE679279C (de) | Verfahren zur Herstellung eines tetraalkylierten Dinitrobenzols | |
| DE270663C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE511211C (de) | Verfahren zur Darstellung von o-Cyanaryirhodanverbindungen | |
| DE123260C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| AT152838B (de) | Verfahren zur Darstellung von Pyridinderivaten. | |
| DE66361C (de) | Verfahren zur Darstellung eines am Azinstickstoff alkylirten Indulins und von Sulfosäuren desselben | |
| AT308070B (de) | Verfahren zur Herstellung von 5-Sulfamyl-4-halogenanthranilsäureaniliden | |
| DE21683C (de) | Verfahren zur Herstellung von Orthonitrometamethylbenzaldehyd aus dem Metamethylbenzaldehyd | |
| DE326486C (de) | Verfahren zur Darstellung der Nitroverbindungen von im aromatischen oder Cyklohexenring durch Hydroxyl- oder Aminogruppen substituierten Tetrahydronaphthalinen und Alkyltetrahydronaphthalinen | |
| DE107509C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE550936C (de) | Verfahren zur Herstellung von Nitro- und Aminoanthrachinonylarylketonen | |
| DE134306C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE767510C (de) | Verfahren zur Herstellung von 1, 3, 5-Trichlor-2, 4, 6-Trinitrobenzol | |
| DE509149C (de) | Verfahren zur Darstellung von kernmethylierten Kohlenwasserstoffen | |
| DE87934C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| DE174238C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |