DE155631C - - Google Patents
Info
- Publication number
- DE155631C DE155631C DENDAT155631D DE155631DA DE155631C DE 155631 C DE155631 C DE 155631C DE NDAT155631 D DENDAT155631 D DE NDAT155631D DE 155631D A DE155631D A DE 155631DA DE 155631 C DE155631 C DE 155631C
- Authority
- DE
- Germany
- Prior art keywords
- chlorophenol
- chlorine
- phenol
- percent
- weight
- 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
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 12
- 239000000460 chlorine Substances 0.000 claims description 12
- 229910052801 chlorine Inorganic materials 0.000 claims description 12
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 10
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims 1
- 239000012442 inert solvent Substances 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 3
- 238000005660 chlorination reaction Methods 0.000 description 3
- 238000004508 fractional distillation Methods 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- ZUJURJDZOPMJPH-UHFFFAOYSA-N 5-diazocyclohexa-1,3-diene;hydrochloride Chemical compound Cl.[N-]=[N+]=C1CC=CC=C1 ZUJURJDZOPMJPH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- -1 benzoyl ester Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 230000002226 simultaneous effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/62—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by introduction of halogen; by substitution of halogen atoms by other halogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
DE155631C true DE155631C (enrdf_load_stackoverflow) |
Family
ID=422085
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DENDAT155631D Active DE155631C (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE155631C (enrdf_load_stackoverflow) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2511784A (en) * | 1950-06-13 | Compositions containing z | ||
DE1213849B (de) * | 1961-04-20 | 1966-04-07 | Dow Chemical Co | Verfahren zur Herstellung von chlorierten Bisphenolen |
-
0
- DE DENDAT155631D patent/DE155631C/de active Active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2511784A (en) * | 1950-06-13 | Compositions containing z | ||
DE1213849B (de) * | 1961-04-20 | 1966-04-07 | Dow Chemical Co | Verfahren zur Herstellung von chlorierten Bisphenolen |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE69011325T2 (de) | Verfahren zur herstellung von dinitrotoluol unter verwendung eines anorganischen salzes als phasentrennmittel. | |
DE155631C (enrdf_load_stackoverflow) | ||
DE69212065T2 (de) | Verfahren zur Reinigung von 2,6-Diisopropylphenol | |
DD158547A5 (de) | Verfahren zur herstellung von alkylsulfochloriden | |
DE2341743B2 (de) | Verfahren zur Herstellung einer Mischung aus Brenzkatechin und Hydrochinon | |
DE1205084B (de) | Verfahren zur Reinigung von rohem, waessrigem Acrylsaeurenitril, welches durch Umsetzung von Acetylen mit Blausaeure entstanden ist | |
DE2614139B2 (de) | Verfahren zur ansatzweisen oder kontinuierlichen Herstellung von o, a, a, a', o ' a '-Hexachlorxylol | |
EP0297238B1 (de) | Verfahren zur Herstellung von Methallylchlorid | |
DE232071C (enrdf_load_stackoverflow) | ||
DE2443341C3 (de) | Verfahren zur Reinigung von Rohcaprolactam | |
DE69020572T2 (de) | Verfahren zur entfernung von chloropren aus 1,2-dichlorethan. | |
DE2208115C3 (de) | Verfahren zur Trennung eines Gemisches von aromatischen Kohlenwasserstoffen, von denen mindestens einer bewegliche Wasserstoffatome aufweist | |
DE2550076B2 (de) | Verfahren zur herstellung von dichlorsilan durch dismutation von trichlorsilan in gegenwart von tetraalkylharnstoff | |
DE898737C (de) | Verfahren zur Herstellung von Chlormethylmethylaether | |
DE2521154A1 (de) | Verfahren zur reingewinnung von styrol aus technischen gemischen | |
DE2113858C3 (de) | Verfahren zur Herstellung von 2,3 Dichlorbutadien-(1,3) | |
DE1812323C3 (de) | Verfahren zur Aufarbeitung von aliphatischen Chlorkohlenwasserstoffen mit 1 bis 4 Kohlenstoffatomen | |
DE1493801C (de) | Kontinuierliches Verfahren zur Her Stellung von Phenol durch Chlorierung von Benzol und Hydrolyse des Chlorbenzols | |
EP0541848B1 (de) | Verfahren zur Abtrennung von Aromaten aus A1C13 enthaltenden Abwässern | |
DE2211060C3 (de) | Verfahren zur Reinigung von Halogenverbindungen enthaltenden 1,4-Dicyanbutenen | |
DE1240057B (de) | Verfahren zur Herstellung von 1, 2, 3, 4-Tetra-chlorbutan | |
DE69004974T2 (de) | Herstellung von 2-Chlorterephthalsäurechlorid. | |
DE1768067B2 (enrdf_load_stackoverflow) | ||
DE1003207B (de) | Verfahren zur Reinigung von nieder-polymere Acetylenverbindungen enthaltendem Acrylsaeurenitril | |
DE738702C (de) | Verfahren zur Herstellung von Polychloralkylaromaten |