DE414146C - Process for the preparation of a red dye - Google Patents

Process for the preparation of a red dye

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Publication number
DE414146C
DE414146C DER60242D DER0060242D DE414146C DE 414146 C DE414146 C DE 414146C DE R60242 D DER60242 D DE R60242D DE R0060242 D DER0060242 D DE R0060242D DE 414146 C DE414146 C DE 414146C
Authority
DE
Germany
Prior art keywords
dye
preparation
red dye
pyridylglycine
aminopyridine
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.)
Expired
Application number
DER60242D
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German (de)
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
FRITZ REINDEL DR
Original Assignee
FRITZ REINDEL DR
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by FRITZ REINDEL DR filed Critical FRITZ REINDEL DR
Priority to DER60242D priority Critical patent/DE414146C/en
Application granted granted Critical
Publication of DE414146C publication Critical patent/DE414146C/en
Expired legal-status Critical Current

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Description

Verfahren zur Darstellung eines roten Farbstoffes. Die Versuche, aus Pyridin zu Farbstoffen zu gelangen, sind nicht zahlreich (Patente 230597, 23o865# 218904, 155782). Es wurde nun gefunden ', daß man das aUS 2-Aminopyridin (Patente 362446 und 374291) und monoch#loressigsaurem Kaäum (oder Natrium) leicht erhältliche Pyridylglycin durch Kochen mit stärkerem Alkali in ausgezeichneter Ausbeute in schwer lösliche Alkalisalze überführen kann, die in wässeriger Lösung durch Oxydation zu roten Farbstoffen führen. Diese sind löslich- in schwachem Ätzalkali und Ammoniak, verdünnten Mineralsäuren und stärkerer Essigsäure und sind gleichzeitig Küpenfarbstoffe. Die Zusammensetzung der entstehenden Farbstoffe ist vermutlich der des Indolindigos analog. Der Weg zum Farbstoff wird demnach durch folgende Formelreihe, wiedergegeben - B e i s p i #e le.Process for the preparation of a red dye. The attempts to get dyes from pyridine are not numerous (patents 230597, 23o865 # 218904, 155782). It has now been found that the aUS 2-aminopyridine (patents 362446 and 374291) and monochloroacetic acid (or sodium) easily obtainable pyridylglycine can be converted in excellent yield into sparingly soluble alkali salts in aqueous solution by boiling with stronger alkali lead to red dyes through oxidation. These are soluble in weak caustic alkali and ammonia, dilute mineral acids and stronger acetic acid and are at the same time vat dyes. The composition of the resulting dyes is presumably analogous to that of the indolinedigo. The way to the dye is represented by the following series of formulas - B ice p i #e le.

i. Zur Darstellung des Pyridylglycins -werden z. B. 30 g Monochloressigsäure in der Kälte in 2oo ccm Wasser,gelöst und mit fester Pottasche oder Soda bis zum Audhören der Kohlensäureentwicklung versetzt. Nach Zufügen von 30 9 2-Aminopyridin und ein-es geringen überschusses an kohlensaurem Alkali (o,5 bis i g) kocht man im Wasserbad 3 bis 4 Stunden. Beim Abkühlen scheidet sich das Pyridylglycin in fast quantitativer Ausbeute ab. - 2. Zur Cberführung in das erwähnte schwer lösliche Alkalisalz kocht man z. B. 2 g Pyridylglycin mit --,o ccm etwa 3oprozentig-er Natronlauge i bis 2 Minuten. Nach dem Ab- kühlen läßt sich das Salz in perlmutterglänzenden weißen Blättch#en isolieren. Ausbeute quantitativ.i. To represent the pyridylglycine z. B. 30 g of monochloroacetic acid in the cold in 2oo ccm of water, dissolved and mixed with solid potash or soda until the development of carbonic acid is heard. After adding 30 g of 2-aminopyridine and a slight excess of carbonate of alkali ( 0.5 to 1 g), the mixture is boiled in a water bath for 3 to 4 hours. On cooling, the pyridylglycine separates out in almost quantitative yield. - 2. To convert into the poorly soluble alkali salt mentioned, one boils z. B. 2 g of pyridylglycine with -, o ccm about 3% sodium hydroxide solution for 1 to 2 minutes. Cool On disconnecting the salt in pearly white Blättch # s can be isolated. Quantitative yield.

3. Für die Gewinnung des Farbstoffes löst man z. B. i g des unter z beschriebenen Natriumsalzes in io ccm Wasser in der Kälte und versetzt mit i o ccm einer I 5prozeritigen Lösung von Kaliumferricyanid. Aus der intensiv gefärbten Lösung kann mit verdünnter, etwa 2oprozeiitiger Essigsäure der Farbstoff gefällt werden. 3. To obtain the dye one solves z. B. i g of the sodium salt described under z in 10 cc of water in the cold and mixed with 10 cc of a 1 5% solution of potassium ferricyanide. The dye can be precipitated from the intensely colored solution with dilute, approximately 20% acetic acid.

Der Farbstoff färbt die Faser aus der Küpe rot; man kann die tierische Faser auch aus saurem Bade mit dem Farbstoff färben; Baumwolle muß vorher mit Tannin und Brechweinstein gebeizt werden.The dye turns the fiber from the vat red; you can get the animal You can also use the dye to dye fibers from an acid bath; Cotton must have tannin beforehand and grape tartar can be pickled.

Claims (1)

PATENT-ANSPRUCH: Verfahren zur Darstellung eines roten Farbstoffes aus 2-Aininopyridin, dadurch, gekennzeichnet, daß man das aus 2-Aminopyridin und Monochloressigsäure leicht erhältliche Pyridylglycin mit Alkali kocht und in wässeriger Lösung zum Farbstoff oxydiert.PATENT CLAIM: Process for the preparation of a red dye from 2-aminopyridine, characterized in that one of 2-aminopyridine and Monochloroacetic acid readily available pyridylglycine boils with alkali and in aqueous Solution oxidized to the dye.
DER60242D 1924-02-01 1924-02-01 Process for the preparation of a red dye Expired DE414146C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DER60242D DE414146C (en) 1924-02-01 1924-02-01 Process for the preparation of a red dye

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DER60242D DE414146C (en) 1924-02-01 1924-02-01 Process for the preparation of a red dye

Publications (1)

Publication Number Publication Date
DE414146C true DE414146C (en) 1925-05-25

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ID=7411284

Family Applications (1)

Application Number Title Priority Date Filing Date
DER60242D Expired DE414146C (en) 1924-02-01 1924-02-01 Process for the preparation of a red dye

Country Status (1)

Country Link
DE (1) DE414146C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1932835A1 (en) * 2005-08-30 2008-06-18 Sumitomo Chemical Company, Limited Method for producing 2,3-dihydropyridazine compound

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1932835A1 (en) * 2005-08-30 2008-06-18 Sumitomo Chemical Company, Limited Method for producing 2,3-dihydropyridazine compound
EP1932835A4 (en) * 2005-08-30 2010-04-28 Sumitomo Chemical Co Method for producing 2,3-dihydropyridazine compound

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