GB1103506A - A process for the production of polyhydrazodicarbonic acid amides or polyureas - Google Patents
A process for the production of polyhydrazodicarbonic acid amides or polyureasInfo
- Publication number
- GB1103506A GB1103506A GB4376264A GB4376264A GB1103506A GB 1103506 A GB1103506 A GB 1103506A GB 4376264 A GB4376264 A GB 4376264A GB 4376264 A GB4376264 A GB 4376264A GB 1103506 A GB1103506 A GB 1103506A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diamine
- hydroxy
- hexanediamine
- groups
- polyureas
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3271—Hydroxyamines
- C08G18/3296—Hydroxyamines being in latent form
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
Polyureas or polyhydrazides containing alcoholic -OH groups are prepared by reacting an aromatic diisocyanate at -20 DEG to +30 DEG C. in an organic solvent with an equivalent amount (i.e. one NCO group per -NH group) of a carbonic or sulphurous acid salt of a diamine or hydrazine containing alcoholic -OH groups, and at least one active hydrogen atom on each of the N atoms. The salt may be prepared in situ by the reaction of SO2 or CO2 with a diamine or hydrazine containing -OH groups. The solvent may be a polar solvent, e.g. dimethyl formamide, dimethylacetamide, N-methyl pyrrolidone, dimethyl sulphoxide or tetramethyl urea. In the examples various diisocyanates were reacted with the salts of (1) N-(b -hydroxypropyl) hexanediamine, (2) N-(b -hydroxybutyl) hexane diamine, (3) N-(b -hydroxy-b -phenylethyl) hexanediamine, (4) N-(b -hydroxy-g -phenoxypropyl) -hexanediamine, (5) N-(b -hydroxy-g -allyloxypropyl) hexane diamine, (6) N-(b -hydroxypropyl) xylylene-1,3-diamine, (7) N1 - [g - (b - hydroxy - b - phenylethyl)] - N - methyl bis propylene diamine, (8) 1,3-diaminopropan-2-ol and (9) b -hydroxyethylhydrazine.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF0041216 | 1963-11-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1103506A true GB1103506A (en) | 1968-02-14 |
Family
ID=7098575
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4376264A Expired GB1103506A (en) | 1963-11-07 | 1964-10-27 | A process for the production of polyhydrazodicarbonic acid amides or polyureas |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE655302A (en) |
GB (1) | GB1103506A (en) |
NL (1) | NL6412960A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4500656A (en) * | 1983-04-05 | 1985-02-19 | Bayer Aktiengesellschaft | Process for the preparation of a cellular polyurethane |
-
1964
- 1964-10-27 GB GB4376264A patent/GB1103506A/en not_active Expired
- 1964-11-05 BE BE655302D patent/BE655302A/xx unknown
- 1964-11-06 NL NL6412960A patent/NL6412960A/xx unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4500656A (en) * | 1983-04-05 | 1985-02-19 | Bayer Aktiengesellschaft | Process for the preparation of a cellular polyurethane |
Also Published As
Publication number | Publication date |
---|---|
NL6412960A (en) | 1965-05-10 |
BE655302A (en) | 1965-03-01 |
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