CH100364A - Process for the preparation of a 1-oxynaphthalene-4-carboxylic acid derivative. - Google Patents
Process for the preparation of a 1-oxynaphthalene-4-carboxylic acid derivative.Info
- Publication number
- CH100364A CH100364A CH100364DA CH100364A CH 100364 A CH100364 A CH 100364A CH 100364D A CH100364D A CH 100364DA CH 100364 A CH100364 A CH 100364A
- Authority
- CH
- Switzerland
- Prior art keywords
- carboxylic acid
- oxynaphthalene
- preparation
- acid derivative
- toluidide
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title claims description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 125000005907 alkyl ester group Chemical group 0.000 claims description 2
- 239000003518 caustics Substances 0.000 claims description 2
- 239000000155 melt Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 claims 1
- 238000000746 purification Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/01—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups
- C07C65/105—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups polycyclic
- C07C65/11—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups polycyclic with carboxyl groups on a condensed ring system containing two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent 1r.99280. Verfahren zur Herstellung eines 1-Ogynaphtalin-4-ear bonsäurederivates. <B>Es</B> wurde gefunden, dass man ein 1-Oxy- naphtalin-4-ca.rbonsäurederivat, das p-Tolui- did der 1-Oxynaphtalin-4-carbonsäure, leicht herstellen kann, wenn man einen Alkylester der 1-Oxynaphtalin-4-carbonsäure mit p-To- Iuidin erhitzt.
Das p-Toluidid der 1-Oxynaph- 1-alin-4-carbonsäure bildet ein farbloses, kri stallinisches Pulver; es schmilzt, aus Methyl- < < lkohol umgelöst, bei 215 und ist in Ätz- alhalien leicht löslich.
<I>Beispiel:</I> 2I)0 Teile 1-Oxynaphtalin-4-carbonsäure- methylester werden mit 500 Teilen p-Tolui- clin 12 Stunden schwach gekocht. Hierauf giesst man in überschüssige, verdünnte Salz- Das ausgeschiedene p-Toluidicl der 1-Oxynaphtalin-4-carbonsäure kann zur Rei nigung aus Methylalkohol umgelöst werden.
Additional patent to main patent 1r.99280. Process for the preparation of a 1-ogynaphtalin-4-ear bonsäurederivates. <B> It </B> has been found that a 1-oxynaphthalene-4-carboxylic acid derivative, the p-toluidide of 1-oxynaphthalene-4-carboxylic acid, can easily be prepared if an alkyl ester is used 1-Oxynaphthalene-4-carboxylic acid heated with p-To-Iuidine.
The p-toluidide of 1-oxynaph-1-alyne-4-carboxylic acid forms a colorless, crystalline powder; when redissolved from methyl alcohol, it melts at 215 and is easily soluble in caustic substances.
<I> Example: </I> 2I) 0 parts of 1-oxynaphthalene-4-carboxylic acid methyl ester are gently boiled with 500 parts of p-toluicine for 12 hours. The precipitated p-toluidicl of 1-oxynaphthalene-4-carboxylic acid can then be redissolved from methyl alcohol for purification.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH100364T | 1922-02-10 | ||
| CH99280T | 1922-02-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH100364A true CH100364A (en) | 1923-07-16 |
Family
ID=25705508
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH100364D CH100364A (en) | 1922-02-10 | 1922-02-10 | Process for the preparation of a 1-oxynaphthalene-4-carboxylic acid derivative. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH100364A (en) |
-
1922
- 1922-02-10 CH CH100364D patent/CH100364A/en unknown
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