CH100359A - Process for the preparation of an aryloxynaphthyl ketone. - Google Patents
Process for the preparation of an aryloxynaphthyl ketone.Info
- Publication number
- CH100359A CH100359A CH100359DA CH100359A CH 100359 A CH100359 A CH 100359A CH 100359D A CH100359D A CH 100359DA CH 100359 A CH100359 A CH 100359A
- Authority
- CH
- Switzerland
- Prior art keywords
- ketone
- oxynaphthyl
- 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 Arylogynaphtylketons. Es wurde gefunden, .dass man ein Aryl- oxynaphtylketon herstellen kann, wenn man auf 1-Oxynaphtalin-8-sulfosäure, mit oder ohne Zusatz von Verdünnungs- bezw. Kon densationsmitteln, aber unter Auss.chluss von Alkalien, Benzotrichlorid einwirken lässt.
Die --o gewonnene 1-Phenylketon-4-oxynaphtyl-5- sulfosäure bildet ein weisses Pulver, welches sich in Ätzalkalien und in konzentrierter Schwefelsäure mit gelber Farbe löst.
<I>Beispiel.:</I> <B>19,5</B> Teile Benzotrichlorid und 22,4 Teile 1.-Oxynaphtalin-8-sulfosäure werden bei Zim mertemperatur in 100 Teile konzentrierte Sehwefelsäure eingetragen und so lange zu- sarnmen gerührt, bis sich keine Salzsäure mehr entwickelt. Hierauf giesst man in Was ser, filtriert die ausgeschiedene 1-Phenyl- l@eton-4-oxynaphtyl-5-sulfosäure ab und rei nigt sie durch L mkristallisieren ihres Na triumsalzes.
Process for the preparation of an arylogynaphthyl ketone. It has been found that an aryl oxynaphthyl ketone can be produced if one responds to 1-oxynaphthalene-8-sulfonic acid, with or without the addition of diluent. Condensation agents, but with the exclusion of alkalis, allows benzotrichloride to act.
The 1-phenylketone-4-oxynaphthyl-5-sulfonic acid obtained forms a white powder that dissolves in caustic alkalis and concentrated sulfuric acid with a yellow color.
<I> Example: </I> <B> 19.5 </B> parts of benzotrichloride and 22.4 parts of 1-oxynaphthalene-8-sulfonic acid are added to 100 parts of concentrated sulfuric acid at room temperature and added for this period. Stirred until no more hydrochloric acid develops. It is then poured into water, the precipitated 1-phenyl-etone-4-oxynaphthyl-5-sulfonic acid is filtered off and purified by crystallizing its sodium salt.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH98559T | 1921-09-24 | ||
CH100359T | 1921-09-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH100359A true CH100359A (en) | 1923-07-16 |
Family
ID=25705430
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH100359D CH100359A (en) | 1921-09-24 | 1921-09-24 | Process for the preparation of an aryloxynaphthyl ketone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH100359A (en) |
-
1921
- 1921-09-24 CH CH100359D patent/CH100359A/en unknown
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