CH215298A - Process for the production of a urea derivative. - Google Patents
Process for the production of a urea derivative.Info
- Publication number
- CH215298A CH215298A CH215298DA CH215298A CH 215298 A CH215298 A CH 215298A CH 215298D A CH215298D A CH 215298DA CH 215298 A CH215298 A CH 215298A
- Authority
- CH
- Switzerland
- Prior art keywords
- urea derivative
- production
- derivative
- hot water
- phosgene
- Prior art date
Links
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
- C07C309/41—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton
- C07C309/42—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton having the sulfo groups bound to carbon atoms of non-condensed six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Harnstoffderioates. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines Harn stoffderivates der Formel
EMI0001.0004
dadurch gekennzeichnet, dass man 3,4-Di- ehloranilin mit Phosgen zu einem Derivat der ;3,4-Dichlorphenylcarbaminsäure und dieses rnit 4-Amino-2,4'-dich@or-3',5'-dimethyl-1,1'- diphenyläther-2'-sulfonsäure umsetzt.
Das neue Ilarnstoffderivat bildet als Natrium- salz ein helles, in heissem Wasser lösliches Pulver und eignet sich als Mottenschutz mittel.
<I>Beispiel:</I> In 500 Teile Essigester, welche 13,5 Teile Phosgen enthalten, wird eine Lösung von 162 Teilen 3,4-Dichloranilin in 1000 Tei len Essigester langsam eingetropft unter gleichzeitigem Durchleiten eines Phosgen- stromes. Nach Beendigung der Reaktion wird das Lösungsmittel im Vakuum bei 30 abdestilliert, wobei das gebildete 3,4-Dichlor- phenylcarbaminsäurechlorid als helles Pulver zurückbleibt.
b) '-/"a Mol. der 4-Am#ino-2;,4'-diehlor-3',5'- dimethyl -1,1' - diphenyläther - 2'- sulfonsäure wird in trockenem Pyridin gelöst und unter Rühren bei 10=15 C portionenweise mit 1/2o Mol. 3,4-Dtichlorphenylearbaminsäurechlo- rid versetzt.
Dann wird bei Raumtemperatur weitergerührt, bis. keine freie Aminogruppe mehr nachweisbar ist. Hierauf versetzt man mit Sodalösung bis zur alkalischen Reaktion und bläst das Pyridin mit Wasserdampf ab. Den Rückstand löst man in heissem Wasser, filtriert die Lösung, fällt das Reaktions produkt durch Zugabe von Ilochsa:z als bräunliches Harz aus und erhält es nach dem Abtrennen, Trocknen und Mahlen als helles, in heissem Wasser lösliches Pulver.
Process for the production of a urea derivative. The subject of the present patent is a process for the preparation of a urea derivative of the formula
EMI0001.0004
characterized in that 3,4-dichloroaniline is mixed with phosgene to form a derivative of; 3,4-dichlorophenylcarbamic acid and this with 4-amino-2,4'-dich @ or-3 ', 5'-dimethyl-1, 1'-diphenyl ether-2'-sulfonic acid converts.
As a sodium salt, the new ilarnea derivative forms a pale powder that is soluble in hot water and is suitable as a moth repellent.
<I> Example: </I> A solution of 162 parts of 3,4-dichloroaniline in 1000 parts of ethyl acetate is slowly added dropwise to 500 parts of ethyl acetate, which contain 13.5 parts of phosgene, while a phosgene stream is passed through at the same time. When the reaction has ended, the solvent is distilled off in vacuo at 30, the 3,4-dichlorophenylcarbamic acid chloride formed remaining as a pale powder.
b) '- / "a mol. of 4-Am # ino-2;, 4'-diehlor-3', 5'-dimethyl -1,1 '- diphenyl ether - 2'-sulfonic acid is dissolved in dry pyridine and under Stirring at 10 = 15 ° C. in portions with 1/2 mol of 3,4-dichlorophenylearbamic acid chloride.
The mixture is then further stirred at room temperature until. no more free amino group can be detected. Soda solution is then added until an alkaline reaction occurs and the pyridine is blown off with steam. The residue is dissolved in hot water, the solution is filtered, the reaction product precipitates out as a brownish resin by adding Ilochsa: z and, after separation, drying and grinding, it is obtained as a pale powder which is soluble in hot water.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH215298T | 1938-06-16 | ||
CH212408T | 1938-06-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH215298A true CH215298A (en) | 1941-06-15 |
Family
ID=25725178
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH215298D CH215298A (en) | 1938-06-16 | 1938-06-16 | Process for the production of a urea derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH215298A (en) |
-
1938
- 1938-06-16 CH CH215298D patent/CH215298A/en unknown
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