IE40263L - Polymerisable o, n-acetals - Google Patents
Polymerisable o, n-acetalsInfo
- Publication number
- IE40263L IE40263L IE241274A IE241274A IE40263L IE 40263 L IE40263 L IE 40263L IE 241274 A IE241274 A IE 241274A IE 241274 A IE241274 A IE 241274A IE 40263 L IE40263 L IE 40263L
- Authority
- IE
- Ireland
- Prior art keywords
- compound
- carbon atoms
- general formula
- alkyl radical
- polyurethane foam
- Prior art date
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims 3
- 229920005830 Polyurethane Foam Polymers 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 239000011496 polyurethane foam Substances 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 claims 1
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
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/638—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers characterised by the use of compounds having carbon-to-carbon double bonds other than styrene and/or olefinic nitriles
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
Claims (9)
- I. A <-<>ni|M>uiii| j My l«> (In- ci'iirral . fornml a (I) in wit iclt X represents hydrogen or an alkyl radical having 1 to 6 carbon atoms; Y represents -Nil-, NC^Il2in+j-(m=l-6) > or -0-; /. represents hydrogen or an alkyl radical having 1 to 4 carbon atoms; represent an alkyl radical having I to l8 carbon atoms or a cycloalkyl radical having 5 to 7 carbon atoms, or R and K', together with the nitrogen atom to which t.hey are attached, may also form a heterocyclic ring optionally containing I'urt her hetero atoms; and is an integer from I lo |(>.
- 2. A process Cor producing a compound ol' the general formula (I) as defined in claim | wherein a <:om|M>und correspond i ng to the loiniu la (II) X is reacted w i I li formaldehyde and a secondary amine coi res|X)iid ing to tlie formula (111) In R and R', which may bo the same or different, each (ii) wherein X, Y, Z and n are as defined in claim I II —N (III) R wherein K and K' are as defined in claim I 40263
- .1. A proccHH um claimed in claim 2, wherein the reaction Lh carried out in the presence of a water-removing agent.
- 4. A process as claimed in claim 2 or 3, wherein the reaction takes place exothermically at a temperature in the range of from 20°C to 100°C.
- 5. A process as claimed in claim 2 .substantially as herein described with reference to any of the specific Exampli 1 to 5.
- 6. A compound of general formula (I) when prepared by the process claimed in any of claims 2 to 5.
- 7. A compound of general formula (I) as defined in claim i substantially as herein described with reference to any of the specific Examples l to 5>
- 8. A polyurethane foam which contains in its structure the residue of at least one compound of the general formula (I) as claimed in any of claim 1,6 and "J.
- 9. A polyurethane foam as claimed in claim 8 substantially as herein described with reference to Example 7. F. R. KELLY & CO. AGENTS FOR THE APPLICANTS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732358761 DE2358761A1 (en) | 1973-11-26 | 1973-11-26 | POLYMERIZABLE O, N-ACETALS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE40263L true IE40263L (en) | 1975-05-26 |
| IE40263B1 IE40263B1 (en) | 1979-04-25 |
Family
ID=5899053
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE241274A IE40263B1 (en) | 1973-11-26 | 1974-11-25 | Polymerisable o,n-acetals |
Country Status (9)
| Country | Link |
|---|---|
| BE (1) | BE822499A (en) |
| DE (1) | DE2358761A1 (en) |
| DK (1) | DK612674A (en) |
| FR (1) | FR2252332B1 (en) |
| GB (1) | GB1441556A (en) |
| IE (1) | IE40263B1 (en) |
| IT (1) | IT1023364B (en) |
| LU (1) | LU71353A1 (en) |
| NL (1) | NL7415349A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2506405A1 (en) * | 1975-02-15 | 1976-08-26 | Agfa Gevaert Ag | PHOTOGRAPHIC SILVER HALOGENIDE EMULSION |
-
1973
- 1973-11-26 DE DE19732358761 patent/DE2358761A1/en active Pending
-
1974
- 1974-11-20 GB GB5018774A patent/GB1441556A/en not_active Expired
- 1974-11-22 BE BE150766A patent/BE822499A/en unknown
- 1974-11-22 IT IT5417874A patent/IT1023364B/en active
- 1974-11-25 DK DK612674A patent/DK612674A/da not_active Application Discontinuation
- 1974-11-25 IE IE241274A patent/IE40263B1/en unknown
- 1974-11-25 LU LU71353A patent/LU71353A1/xx unknown
- 1974-11-25 NL NL7415349A patent/NL7415349A/en unknown
- 1974-11-26 FR FR7438684A patent/FR2252332B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2358761A1 (en) | 1975-06-05 |
| LU71353A1 (en) | 1975-08-20 |
| BE822499A (en) | 1975-05-22 |
| FR2252332A1 (en) | 1975-06-20 |
| DK612674A (en) | 1975-07-28 |
| FR2252332B1 (en) | 1978-06-16 |
| GB1441556A (en) | 1976-07-07 |
| IT1023364B (en) | 1978-05-10 |
| IE40263B1 (en) | 1979-04-25 |
| NL7415349A (en) | 1975-05-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES8405398A1 (en) | Diazabicyclo(3.3.1)nonanes. | |
| ES8407025A1 (en) | New herbicidal nicotinamide derivatives. | |
| IE883845L (en) | Adenosine derivative | |
| MX9606331A (en) | Novel compound, process for producing the same, and antitumor agent. | |
| GB1213779A (en) | Production of organo-silicon compounds | |
| JPS5498711A (en) | Novel easily decomposable anti-cholinergic, anti-secretic compound and pharmaceutical composition containing the same | |
| DE3372095D1 (en) | Novel phenylpiperazine derivatives and process for producing the same | |
| MY104455A (en) | Preparation of 1,4-diazabicyclo [3.2.2] nonane. | |
| IE40263L (en) | Polymerisable o, n-acetals | |
| CA2021733A1 (en) | Azole-substituted cycloalkanol derivative, a process to produce the same and a use of the derivative as an agricultural and horticultural fungicide | |
| MY108849A (en) | Novel compound | |
| ES8103106A1 (en) | Process for the preparation of diorganomagnesium compounds. | |
| CA2020995A1 (en) | Process for decomposition of methanol | |
| MY106383A (en) | Process for preparing ergoline derivatives. | |
| ES8304971A1 (en) | Process for the preparation of azabicyclo(3.2.0)-hept-2-ene derivatives. | |
| EP0031388A4 (en) | Process for preparing imidazole derivatives. | |
| CH609692A5 (en) | Process for the preparation of new piperazinopyrimidines | |
| DE3063380D1 (en) | Process for preparing oxiranes | |
| JPS6480434A (en) | Pigment dispersant | |
| ES8103736A1 (en) | 5,10-Dioxo-5,10-dihydrodiimidazo(1,5-a,1',5'-d)pyrazine-1,6-dicarboxylic acid and a process for producing imidazoledicarboxylic acid amido-derivatives. | |
| ES453664A1 (en) | 5-Amino or substituted amino-7-phenyl or substituted phenyl-2,3-dihydro-1H-1,4-diazepines | |
| ES8201962A1 (en) | Novel 1,1,3,5-substituted biuret compound and a pharmaceutical composition containing the same | |
| GB1475513A (en) | Benzylamine derivatives process for science union et cie benzylamine derivatives process for their production and pharmaceutical compositions containing them | |
| AU534862B2 (en) | Benzazepine derivatives | |
| ES449705A1 (en) | Antimicrobial pyridthiones |