CH256765A - Process for the production of a new half-ester. - Google Patents
Process for the production of a new half-ester.Info
- Publication number
- CH256765A CH256765A CH256765DA CH256765A CH 256765 A CH256765 A CH 256765A CH 256765D A CH256765D A CH 256765DA CH 256765 A CH256765 A CH 256765A
- Authority
- CH
- Switzerland
- Prior art keywords
- ester
- new half
- production
- acid
- new
- Prior art date
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/08—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/593—Dicarboxylic acid esters having only one carbon-to-carbon double bond
- C07C69/60—Maleic acid esters; Fumaric acid esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
- C07C69/80—Phthalic acid esters
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 248209. Verfahren zur Herstellung eines neuen Halbesters. Es wurde gefunden, dass man zu einem neuen Halbester gelangt, wenn man 1 Mol Stearinsäure-ss-oxyäthylester mit 1 Mol Malein- säure oder Maleinsäureanhydrid umsetzt.
Es ist vorteilhafter, Maleinsäureanhydrid als Maleinsäure selbst zu verwenden.
Die Umsetzung wird zweckmässig in der Wärme, z. B. bei 90 bis 120 , vorgenommen. Nenn man Maleinsäure als Ausgangsstoff verwendet, ist es vorteilhaft, unter Zusatz einer geringen Menge einer starken Säure mit dem Stearinsäure-ss-oxyäthylester zu erhitzen, bis 1 Mol Wasser abgespalten ist.
Das Natriumsalz des neuen Halbesters bil det eine annähernd farblose, in warmem Was ser schäumend lösliche Masse. Es kann als Textilhilfsmittel verwendet werden.
Beispiel: Man erhitzt<B>6,3</B> Teile S,tearinsäure-ss-oxy- äthylester und 2,1 Teile Maleinsäureanhydrid unter Rühren während etwa <B>3</B> Stunden auf 95 bis 100 , löst das Veresterungsgemisch in Äthylalkohol, neutralisiert mit verdünnter Natriumhydroxydlösung und dampft zur Trockne ein. Das so erhaltene neue Natrium salz, das durch Extraktion mit Aceton von einer geringen Menge eines Nebenproduktes befreit werden kann, bildet eine annähernd farblose, in warmem Wasser schäumend lös liche Masse.
Es kann als Textilhilfsmittel ; verwendet werden.
<B> Additional patent </B> to main patent No. 248209. Process for the production of a new half-ester. It has been found that a new half ester is obtained if 1 mole of stearic acid ss-oxyethyl ester is reacted with 1 mole of maleic acid or maleic anhydride.
It is more beneficial to use maleic anhydride than maleic acid itself.
The implementation is expediently in the heat, for. B. at 90 to 120 made. If maleic acid is used as the starting material, it is advantageous, with the addition of a small amount of a strong acid, to heat the stearic acid ss-oxyethyl ester until 1 mol of water has been split off.
The sodium salt of the new half-ester forms an almost colorless mass that foams and dissolves in warm water. It can be used as a textile auxiliary.
Example: One heats <B> 6.3 </B> parts of S, tearic acid-ss-oxy-ethyl ester and 2.1 parts of maleic anhydride with stirring for about <B> 3 </B> hours to 95 to 100, this dissolves Esterification mixture in ethyl alcohol, neutralized with dilute sodium hydroxide solution and evaporated to dryness. The new sodium salt obtained in this way, which can be freed from a small amount of a by-product by extraction with acetone, forms an almost colorless mass that foams in warm water.
It can be used as a textile auxiliary; be used.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH248209T | 1945-04-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH256765A true CH256765A (en) | 1948-08-31 |
Family
ID=4466750
Family Applications (6)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH256764D CH256764A (en) | 1945-04-09 | 1945-04-09 | Process for the production of a new half-ester. |
CH248209D CH248209A (en) | 1945-04-09 | 1945-04-09 | Process for the production of a new half-ester. |
CH256765D CH256765A (en) | 1945-04-09 | 1945-04-09 | Process for the production of a new half-ester. |
CH256767D CH256767A (en) | 1945-04-09 | 1946-02-27 | Process for the production of a new half-ester. |
CH256763D CH256763A (en) | 1945-04-09 | 1946-02-27 | Process for the production of a new half-ester. |
CH256766D CH256766A (en) | 1945-04-09 | 1946-02-27 | Process for the production of a new half-ester. |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH256764D CH256764A (en) | 1945-04-09 | 1945-04-09 | Process for the production of a new half-ester. |
CH248209D CH248209A (en) | 1945-04-09 | 1945-04-09 | Process for the production of a new half-ester. |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH256767D CH256767A (en) | 1945-04-09 | 1946-02-27 | Process for the production of a new half-ester. |
CH256763D CH256763A (en) | 1945-04-09 | 1946-02-27 | Process for the production of a new half-ester. |
CH256766D CH256766A (en) | 1945-04-09 | 1946-02-27 | Process for the production of a new half-ester. |
Country Status (2)
Country | Link |
---|---|
CH (6) | CH256764A (en) |
ES (1) | ES173132A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1039057B (en) * | 1951-11-08 | 1958-09-18 | Pittsburgh Coke & Chemical Com | Process for the preparation of fungicidally active alkyl esters of N- (phenyl) maleamic acids |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3528939A (en) * | 1968-01-22 | 1970-09-15 | Sinclair Research Inc | Water dispersible half esters of styrenemaleic anhydride copolymers with n-hydroxy alkyl amides of unsaturated fat acids |
CN117285692A (en) * | 2023-09-14 | 2023-12-26 | 广州敬信高聚物科技有限公司 | Modified TPU material with good flexibility, preparation method and application thereof |
-
1945
- 1945-04-09 CH CH256764D patent/CH256764A/en unknown
- 1945-04-09 CH CH248209D patent/CH248209A/en unknown
- 1945-04-09 CH CH256765D patent/CH256765A/en unknown
-
1946
- 1946-02-27 CH CH256767D patent/CH256767A/en unknown
- 1946-02-27 CH CH256763D patent/CH256763A/en unknown
- 1946-02-27 CH CH256766D patent/CH256766A/en unknown
- 1946-04-06 ES ES173132A patent/ES173132A1/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1039057B (en) * | 1951-11-08 | 1958-09-18 | Pittsburgh Coke & Chemical Com | Process for the preparation of fungicidally active alkyl esters of N- (phenyl) maleamic acids |
Also Published As
Publication number | Publication date |
---|---|
CH248209A (en) | 1947-04-30 |
CH256767A (en) | 1948-08-31 |
ES173132A1 (en) | 1946-05-16 |
CH256766A (en) | 1948-08-31 |
CH256764A (en) | 1948-08-31 |
CH256763A (en) | 1948-08-31 |
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