CH100360A - Process for the preparation of an aryloxynaphthyl ketone. - Google Patents
Process for the preparation of an aryloxynaphthyl ketone.Info
- Publication number
- CH100360A CH100360A CH100360DA CH100360A CH 100360 A CH100360 A CH 100360A CH 100360D A CH100360D A CH 100360DA CH 100360 A CH100360 A CH 100360A
- Authority
- CH
- Switzerland
- Prior art keywords
- ketone
- oxynaphthalene
- sulfonic acid
- benzotrichloride
- act
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/82—Ketones containing a keto group bound to a six-membered aromatic ring containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Aryloxynaphtylketous. Es wurde gefunden, dass man ein Aryl- oxynaphtylketon herstellen kann, wenn man auf 2-Oxynaphtalin-6-sulfosäure, mit oder ohne Zusatz von Verdünnungs- bezw. Kon densationsmitteln, aber unter Ausschluss von Alkalien, Benzotrichlorid einwirken lässt. Die so gewonnene 1-Phenylketon-2-oxynaphtalin- 6-sulfosäure bildet ein weisses Pulver, welches sich in Atzalkalien und in konzentrierter Schwefelsäure mit gelber Farbe löst.
<I>Beispiel:</I> 19,5 Teile Benzotrichlorid und 22,4 Teile 2-Oxynaphtalin-6-sulfosäure werden bei Zim mertemperatur in 100 Teile konzentrierte Schwefelsäure eingetragen und so lange zu sammen gerührt, bis sich keine Salzsäure mehr entwickelt. Hierauf giesst man in Was ser, filtriert die ausgeschiedene 1-Phenyl- keton-2-oxynaphtalin-6-sulfosäure ab und rei nigt sie durch Umkristallisieren ihres Na triumsalzes.
Process for the preparation of an aryloxynaphthylketous. It has been found that an aryl oxynaphtyl ketone can be produced if one responds to 2-oxynaphthalene-6-sulfonic acid, with or without the addition of diluent. Condensation agents, but with the exclusion of alkalis, benzotrichloride can act The 1-phenylketone-2-oxynaphthalene-6-sulfonic acid obtained in this way forms a white powder which dissolves in caustic alkalis and in concentrated sulfuric acid with a yellow color.
<I> Example: </I> 19.5 parts of benzotrichloride and 22.4 parts of 2-oxynaphthalene-6-sulfonic acid are added to 100 parts of concentrated sulfuric acid at room temperature and stirred together until hydrochloric acid no longer develops. This is then poured into water, the precipitated 1-phenyl ketone-2-oxynaphthalene-6-sulfonic acid is filtered off and it is purified by recrystallizing its sodium salt.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH98559T | 1921-09-24 | ||
CH100360T | 1921-09-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH100360A true CH100360A (en) | 1923-07-16 |
Family
ID=25705431
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH100360D CH100360A (en) | 1921-09-24 | 1921-09-24 | Process for the preparation of an aryloxynaphthyl ketone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH100360A (en) |
-
1921
- 1921-09-24 CH CH100360D patent/CH100360A/en unknown
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