AT35554B - Process for the preparation of methylenzitryl cresotinic acids. - Google Patents
Process for the preparation of methylenzitryl cresotinic acids.Info
- Publication number
- AT35554B AT35554B AT35554DA AT35554B AT 35554 B AT35554 B AT 35554B AT 35554D A AT35554D A AT 35554DA AT 35554 B AT35554 B AT 35554B
- Authority
- AT
- Austria
- Prior art keywords
- methylenzitryl
- preparation
- cresotinic acids
- acid
- cresotinic
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims description 5
- 150000007513 acids Chemical class 0.000 title claims 2
- 238000000034 method Methods 0.000 title claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
<Desc/Clms Page number 1>
EMI1.1
EMI1.2
<Desc/Clms Page number 2>
EMI2.1
in Wasser und Petroläther fast unlöslich, in Azeton, Alkohol und Essigsäure leicht löslich sind.
Der Schmelzpunkt liegt unscharf bei 1700 unter Zersetzung.
Beispiel 6 : 304 Teile Oxy-o-toluylsäure (OH : ODOR : CH3 : 3) werden in Chloroform gelöst, mit 300 Teilen Chinolin versetzt und eine Lösung von 241 Teilen Methylen- xitionensä. urcdichlorid in Chloroform unter Rühren zugefiigt. Die Reaktion beginnt sofort unter Temperaturerhöhung. Nach mehrst. undigem Stehen wird die Reaktionsmasse durch Waschen mit salzsäurehaltigem Wasser von Chinolin befreit. Hierbei scheidet sich ein Teil der Methylenzitryl-oxytoluylsäure ab, der Rest wird durch Abdestillieren des Chloroforms gewonnen. Zur
EMI2.2
löslich sind, dagegen sich leicht in Alkohol und Eisessig auflösen. Der Körper schmilzt unscharf bei 170-1750.
In analoger Weise verläuft die Reaktion bei Verwendung anderer Dihalogenide der Met, Ìtylenzitronensäure.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
EMI1.1
EMI1.2
<Desc / Clms Page number 2>
EMI2.1
are almost insoluble in water and petroleum ether, easily soluble in acetone, alcohol and acetic acid.
The melting point is indistinct at 1700 with decomposition.
Example 6: 304 parts of oxy-o-toluic acid (OH: ODOR: CH3: 3) are dissolved in chloroform, 300 parts of quinoline are added and a solution of 241 parts of methylene xionite acid is added. urcdichlorid in chloroform with stirring. The reaction begins immediately with an increase in temperature. After several. After standing, the reaction mass is freed from quinoline by washing with water containing hydrochloric acid. Part of the methylenzitryl-oxytoluic acid separates out, the remainder is obtained by distilling off the chloroform. To
EMI2.2
are soluble, but easily dissolve in alcohol and glacial acetic acid. The body melts out of focus at 170-1750.
The reaction proceeds in an analogous manner when using other dihalides of Met, Ìtylenic citric acid.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1906193114D DE193114C (en) | 1906-10-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT35554B true AT35554B (en) | 1908-12-28 |
Family
ID=5737444
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT35554D AT35554B (en) | 1906-10-19 | 1907-12-16 | Process for the preparation of methylenzitryl cresotinic acids. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT35554B (en) |
-
1907
- 1907-12-16 AT AT35554D patent/AT35554B/en active
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