GB794061A - Manufacture of polyurethane materials - Google Patents
Manufacture of polyurethane materialsInfo
- Publication number
- GB794061A GB794061A GB3380855A GB3380855A GB794061A GB 794061 A GB794061 A GB 794061A GB 3380855 A GB3380855 A GB 3380855A GB 3380855 A GB3380855 A GB 3380855A GB 794061 A GB794061 A GB 794061A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloromethyl
- bis
- cyanate
- stands
- benzene
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
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
A process for the manufacture of polyurethanes comprises reacting together a metal cyanate or mixture of metal cyanates, a polyhydric alcohol or mixture of polyhydric alcohols and a compound or compounds of the formula X-CH2-R-CH3-X wherein stands for -Cl, -Br, -I or -OSO2R1, where R1 stands for a monovalent hydrocarbon radical, and R stands for a divalent substituted or unsubstituted hydrocarbon residue. Reactants specified are sodium and potassium cyanates; ethylene glycol, hexamethylene glycol, decamethylene glycol, glycerol, pentaerythritol and hexantriol; ethylene dibromide, 1 : 4-dibromobutene-2, 1,4-dibromobutane, and compounds where R stands for a divalent aryl residue which may be further substituted, e.g. by methyl chlorine, such as 1 : 4-bis (chloromethyl) benzene and 1 : 4- or 1 : 5-bis(chloromethyl)-naphthalene. The reactants are heated together preferably in such quantities that there is at least one molecule of metal cyanate and at least one hydroxyl group present for each of the groups X. Suitable reaction media are dimethyl sulphoxide and organic amides derived from secondary amines of the type used in Specification 610,117, [Group IV (b)], e.g. dimethylformamide and N-isopropylphthalimidine. The products may be precipitated by cooling and, if necessary, adding a diluent such as water. Examples describe the preparation of polymeric products by heating together in dimethylformamide or dimethyl sulphoxide mixtures of (1) and (2) 1 : 4-bis(chloromethyl) benzene, sodium cyanate and ethylene glycol; (3) 4 : 6 - bis - (chloromethyl) - 1 : 3 - dimethylbenzene, sodium cyanate and ethylene glycol; (4) lead cyanate, 1 : 4-bis-(chloromethyl)-benzene and ethylene glycol; (5) 1 : 4-bis-(chloromethyl)-benzene, sodium cyanate and pentane-1 : 5-diol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3380855A GB794061A (en) | 1955-11-25 | 1955-11-25 | Manufacture of polyurethane materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3380855A GB794061A (en) | 1955-11-25 | 1955-11-25 | Manufacture of polyurethane materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB794061A true GB794061A (en) | 1958-04-30 |
Family
ID=10357702
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3380855A Expired GB794061A (en) | 1955-11-25 | 1955-11-25 | Manufacture of polyurethane materials |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB794061A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3526624A (en) * | 1966-03-04 | 1970-09-01 | Marathon Oil Co | Production of urethane-containing compositions |
US3526623A (en) * | 1965-12-17 | 1970-09-01 | Marathon Oil Co | Urethane drying oils |
-
1955
- 1955-11-25 GB GB3380855A patent/GB794061A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3526623A (en) * | 1965-12-17 | 1970-09-01 | Marathon Oil Co | Urethane drying oils |
DE1645037B1 (en) * | 1965-12-17 | 1971-02-25 | Marathon Oil Co | Process for making desiccant urethanoels |
US3526624A (en) * | 1966-03-04 | 1970-09-01 | Marathon Oil Co | Production of urethane-containing compositions |
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