AT81072B - Process for the preparation of p-chlorophenol. Process for the preparation of p-chlorophenol. - Google Patents
Process for the preparation of p-chlorophenol. Process for the preparation of p-chlorophenol.Info
- Publication number
- AT81072B AT81072B AT81072DA AT81072B AT 81072 B AT81072 B AT 81072B AT 81072D A AT81072D A AT 81072DA AT 81072 B AT81072 B AT 81072B
- Authority
- AT
- Austria
- Prior art keywords
- chlorophenol
- preparation
- dichlorobenzene
- acid
- sulfuric acid
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Darstellung von p-Chlorphenol.
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selbst mit Schwefelsäure bestimmter Konzentration (Mischung gleicher Teile Wasser und Schwefelsäure von 660 Bé) unter Rückfluss kocht, wobei in sehr guter Ausbeute p-Chlorphenol erhalten wird. Da die durch Sulfiren von p-Dichlorbenzol in bekannter Weise leicht erhältliche p-Dichlorbenzolsäure mit verdünnter Natronlauge unter Druck bekannt Ich glatt in die p-Clilorphenolsulfosiiure übergeht, ist mit der beschriebenen Reaktion ein einfacher Weg vom p-Dichlorbenzol zu dem wertvollen p-Chlorphenol gegeben. Es war zwar schon bekannt, dass man die Sulfogruppe aus o-Chlorphenolsulfosäure abspalten kann (vergl. D. R. P. Nr. 141751).
Nach diesem Verfahren wird die Abspaltung aber bei höherer
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fahren das Arbeiten in offenen Gefässen.
Beispiel : 100 kg p-chlorphenolsulfosaures Natrium werden mit 1000 l einer Mischung
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keine Zunahme der sich bald abscheidenden, öligen Schicht von p-Chlorphenol mehr festzustellen ist. Hierauf trennt man das dunkelgef bte Öl nach dem Erkalten von der schwefelsauren Unterlage ab, trocknet und destilliert es in der Kolonne. wobei ohne jeden Vorlauf über 210 das p-Chlorphenol innerhalb von zwei Graden übergeht. Es erstarrt manchmal von selbst, sicher beim Abkühlen und Impfen zu schneeweissen Kristallen.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
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Process for the preparation of p-chlorophenol.
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boils under reflux even with sulfuric acid of a certain concentration (mixture of equal parts of water and sulfuric acid of 660 Bé), whereby p-chlorophenol is obtained in very good yield. Since p-dichlorobenzene acid, which is easily obtainable in a known manner by sulphuring p-dichlorobenzene with dilute sodium hydroxide solution under pressure, is known to convert smoothly into p-clilophenol sulfonic acid, the reaction described provides a simple route from p-dichlorobenzene to valuable p-chlorophenol . It was already known that the sulfo group can be split off from o-chlorophenolsulfonic acid (cf. D. R. P. No. 141751).
However, according to this process, the elimination is higher
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drive working in open vessels.
Example: 100 kg of p-chlorophenolsulfonate are mixed with 1000 l of a mixture
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no increase in the soon-to-be-deposited, oily layer of p-chlorophenol can be observed. The dark colored oil is then separated from the sulfuric acid base after cooling, dried and distilled in the column. the p-chlorophenol passing over within two degrees without any run above 210. It sometimes freezes by itself, certainly when cooling and seeding, to snow-white crystals.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT81072T | 1917-11-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT81072B true AT81072B (en) | 1920-08-10 |
Family
ID=3602587
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT81072D AT81072B (en) | 1917-11-21 | 1917-11-21 | Process for the preparation of p-chlorophenol. Process for the preparation of p-chlorophenol. |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT81072B (en) |
-
1917
- 1917-11-21 AT AT81072D patent/AT81072B/en active
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