CH134841A - Process for the preparation of an arylaminonaphthalene derivative. - Google Patents
Process for the preparation of an arylaminonaphthalene derivative.Info
- Publication number
- CH134841A CH134841A CH134841DA CH134841A CH 134841 A CH134841 A CH 134841A CH 134841D A CH134841D A CH 134841DA CH 134841 A CH134841 A CH 134841A
- Authority
- CH
- Switzerland
- Prior art keywords
- compound
- arylaminonaphthalene
- derivative
- preparation
- amino
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000012670 alkaline solution Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 238000001802 infusion Methods 0.000 claims description 2
- 239000013067 intermediate product Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Description
Verfahren zur Darstellung eines Arylaminonaphtalinderivates. Anaiog dem im Hauptpatent<B>132030</B> be,- schriebenen Verfahren erhält man das 2<B>-</B> 7- Di-(4'-o.xyphenylamiilo)-naplitalin,
wenn man 2<B>-</B> 7-Dioxyna.phialin und 4-Amino-l-oxyben- z o <B>'</B> l in Geo-enwart von Bisulfitlauge mit oder ohne Anwendung von Druck auf höhere Tem peratur erhitzt,.
<I>Beispiel:</I> <B>160</B> Teile 2<B>-</B> 7-Dioxynaphia.Iin werden in einem verbleiten Rührkessel mit einer Lö sung von 400 Teilen Alkalibisulfit in<B>3000</B> Teilen Wasser und<B>260</B> Teilen 4-Amino-l- oxybenzol etwa 120 Stunden lang unter Rückfluss gekocht. Nach dem Abkühlen auf etwa<B>70 '</B> presst man das in hellgrauen Kri stallen auso-eschiedene 2 .7-Di(4'-oxyphenyl- amino)-Naphtalin ab und wäscht es mit heissem Wasser.
Die getrocknete und in guter Ausbeute erhaltene Verbinduno, <B>I</B> el schmilzt bei 249 bis 2151 <B>' C.</B>
Die Verbindung ist löslich in heissem Alkohol und in verdünnten Alkalien. Ein Aufguss der wässerigen alkalischen Lösung auf Papier liefert beim Betupfen mit Chlar- lauo-e eine blaurote Färbung. Die Verbin dung ist ein Zwiselienprodukt für :die Her stellung von Farbstoffen.
Process for the preparation of an arylaminonaphthalene derivative. Analogous to the process described in the main patent <B> 132030 </B>, the 2 <B> - </B> 7- di- (4'-o.xyphenylamiilo) -naplitalin is obtained,
if you have 2 <B> - </B> 7-Dioxyna.phialin and 4-Amino-l-oxyben- zo <B> '</B> l in Geo-enwart of bisulfite liquor with or without application of pressure to higher tem temperature heated.
<I> Example: </I> <B> 160 </B> parts 2 <B> - </B> 7-Dioxynaphia.Iin are in a leaded stirred tank with a solution of 400 parts of alkali bisulfite in <B> 3000 </B> Parts of water and <B> 260 </B> parts of 4-amino-l-oxybenzene are refluxed for about 120 hours. After cooling to about <B> 70 '</B>, the 2 .7-di (4'-oxyphenylamino) naphthalene, which is precipitated in light gray crystals, is pressed off and washed with hot water.
The dried compound obtained in good yield, <B> I </B> el, melts at 249 to 2151 <B> 'C. </B>
The compound is soluble in hot alcohol and in dilute alkalis. An infusion of the aqueous alkaline solution on paper produces a bluish-red color when dabbed with Chlar- lauo-e. The compound is an intermediate product for: the manufacture of dyes.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE134841X | 1926-12-13 | ||
| CH132030T | 1927-12-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH134841A true CH134841A (en) | 1929-08-15 |
Family
ID=25711750
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH134841D CH134841A (en) | 1926-12-13 | 1927-12-03 | Process for the preparation of an arylaminonaphthalene derivative. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH134841A (en) |
-
1927
- 1927-12-03 CH CH134841D patent/CH134841A/en unknown
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