CH187901A - Process for the preparation of 2-amino-1-oxynaphthalene-6-sulfonic acid. - Google Patents
Process for the preparation of 2-amino-1-oxynaphthalene-6-sulfonic acid.Info
- Publication number
- CH187901A CH187901A CH187901DA CH187901A CH 187901 A CH187901 A CH 187901A CH 187901D A CH187901D A CH 187901DA CH 187901 A CH187901 A CH 187901A
- Authority
- CH
- Switzerland
- Prior art keywords
- amino
- oxynaphthalene
- acid
- acids
- sulfonic acid
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 5
- 238000002360 preparation method Methods 0.000 title description 2
- 239000002253 acid Substances 0.000 claims description 17
- 150000007513 acids Chemical class 0.000 claims description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 7
- 239000012736 aqueous medium Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000000975 dye Substances 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000013067 intermediate product Substances 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XHUGGWPQJIAFHM-UHFFFAOYSA-N S(=O)(=O)(O)C(=O)O.C1=CC=CC=C1 Chemical class S(=O)(=O)(O)C(=O)O.C1=CC=CC=C1 XHUGGWPQJIAFHM-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/49—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
- C07C309/50—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms having at least one of the sulfo groups bound to a carbon atom of a six-membered aromatic ring being part of a condensed ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung von 2-Amino-l-ogynaphthalin-6-sulfonsäure. Es wurde gefunden, dass die 2-Amino-l- oxynaphthalin-6-sulfonsäure hergestellt wer den kann, wenn 2-Amino-l-oxynaphthalin- 4. 6-disulfonsäure in wässerigem Medium mit Säuren erhitzt wird.
Die 2-Amino-l-oxynaphthalin-6-sulfon- säure stellt ein farbloses Pulver dar, das in kaltem Wasser und in verdünnten Säuren ziemlich schwer löslich ist, während es sich in verdünnten Alkalien mit olivgrüner Farbe, die an der Luft allmählich dunkler wird, löst. Sie stellt ein wertvolles Zwischenprodukt zur Herstellung von Farbstoffen dar.
Als Säuren, mit denen die 2-Amino-l- oxynaphthalin-4.6-disulfonsäure in wässeri gem Medium erhitzt und dabei die sich in 4-Stellung befindende Sulfonsäuregruppedurch Wasserstoff ersetzt werden kann,, kommen anorganische Säuren sowie aromatische und hydroaromatische Säuren in Betracht;
solche Säuren sind zum Beispiel Salzsäure, Schwefel säure, Phosphorsäure, Benzol- sowie Naphtha linmono-, -di- und polysulfonsäuren, Benzol- sulfocarbonsäuren und Tetrabydronapbtbalin- sulfonsäuren. Eine besonders glatte Umsetzung lässt sich bei Verwendung von verdünnten Mineralsäuren erzielen, und von diesen eignet sich verdünnte Schwefelsäure besonders gut.
Das Erhitzen der 2-Amino-l-oxynaphtha- lin-4. 6-disulfonsäure in wässerigem Medium mit Säuren kann offen oder unter Druck, in Gegenwart oder Abwesenheit von organischen Lösungs- oder Siispensionsmitteln, wie zum Beispiel Alkohol, erfolgen.
<I>Beispiel:</I> 32 Teile 2-Amino-l-oxynaphtbalin-4.6- disulfonsäure werden in 200 Teilen Wasser gelöst; zu dieser Lösung gibt man 200 Teile konzentrierte Schwefelsäure und kocht 30 Stunden am Rückflusskühler. Hierauf lässt man erkalten, wobei die 2-Amino-l-oxyiiaph- thalin-6-sulfonsäure in kristallisierter Form ausfällt. Sie wird abfiltriert, gewaschen und getrocknet.
Process for the preparation of 2-amino-1-ogynaphthalene-6-sulfonic acid. It has been found that 2-amino-l-oxynaphthalene-6-sulfonic acid can be produced when 2-amino-1-oxynaphthalene-4, 6-disulfonic acid is heated with acids in an aqueous medium.
2-Amino-1-oxynaphthalene-6-sulfonic acid is a colorless powder which is rather sparingly soluble in cold water and in dilute acids, while in dilute alkalis it is olive-green in color, which gradually darkens in the air , solves. It is a valuable intermediate product in the manufacture of dyes.
The acids with which the 2-amino-l-oxynaphthalene-4,6-disulfonic acid can be heated in an aqueous medium and the sulfonic acid group in the 4-position can be replaced by hydrogen are inorganic acids and aromatic and hydroaromatic acids;
such acids are, for example, hydrochloric acid, sulfuric acid, phosphoric acid, benzene and naphtha linmono-, di- and polysulphonic acids, benzene sulphocarboxylic acids and tetrabydronapbtbalin sulphonic acids. A particularly smooth conversion can be achieved using dilute mineral acids, and of these, dilute sulfuric acid is particularly suitable.
Heating the 2-amino-l-oxynaphthalin-4. 6-disulfonic acid in an aqueous medium with acids can be carried out openly or under pressure, in the presence or absence of organic solvents or suspending agents, such as alcohol.
<I> Example: </I> 32 parts of 2-amino-1-oxynaphthalene-4,6-disulfonic acid are dissolved in 200 parts of water; 200 parts of concentrated sulfuric acid are added to this solution and the mixture is refluxed for 30 hours. It is then allowed to cool, with the 2-amino-1-oxyiiaphthalene-6-sulfonic acid precipitating in crystallized form. It is filtered off, washed and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH187901T | 1934-12-18 | ||
| CH181530T | 1934-12-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH187901A true CH187901A (en) | 1936-11-30 |
Family
ID=25720543
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH187901D CH187901A (en) | 1934-12-18 | 1934-12-18 | Process for the preparation of 2-amino-1-oxynaphthalene-6-sulfonic acid. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH187901A (en) |
-
1934
- 1934-12-18 CH CH187901D patent/CH187901A/en unknown
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