GB886460A - Improvements in or relating to the manufacture of aromatic ethers - Google Patents
Improvements in or relating to the manufacture of aromatic ethersInfo
- Publication number
- GB886460A GB886460A GB23698/60A GB2369860A GB886460A GB 886460 A GB886460 A GB 886460A GB 23698/60 A GB23698/60 A GB 23698/60A GB 2369860 A GB2369860 A GB 2369860A GB 886460 A GB886460 A GB 886460A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenol
- alkenyl
- ethers
- catalyst
- butenyl
- 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
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 150000008378 aryl ethers Chemical class 0.000 title 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 6
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 4
- -1 alkenyl ether Chemical compound 0.000 abstract 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract 4
- 150000001993 dienes Chemical class 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 3
- 229910015900 BF3 Inorganic materials 0.000 abstract 2
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- 150000001335 aliphatic alkanes Chemical class 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 abstract 2
- 229920000647 polyepoxide Polymers 0.000 abstract 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 abstract 1
- WHGLCGDQDOOABC-UHFFFAOYSA-N 1-but-1-enoxy-3-[1-(2-but-1-enoxyphenyl)butyl]-2-but-1-enylbenzene Chemical compound C(=CCC)OC1=C(C=CC=C1)C(CCC)C1=C(C(=CC=C1)OC=CCC)C=CCC WHGLCGDQDOOABC-UHFFFAOYSA-N 0.000 abstract 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 abstract 1
- FHQBZLCAJCGWKV-ZZXKWVIFSA-N 2-[(e)-but-1-enyl]phenol Chemical compound CC\C=C\C1=CC=CC=C1O FHQBZLCAJCGWKV-ZZXKWVIFSA-N 0.000 abstract 1
- CWAKODPIAKUIAI-UHFFFAOYSA-N C(=CCC)OC1=C(C=CC=C1)C(C(C)C1=C(C=CC=C1)OC=CCC)C Chemical compound C(=CCC)OC1=C(C=CC=C1)C(C(C)C1=C(C=CC=C1)OC=CCC)C CWAKODPIAKUIAI-UHFFFAOYSA-N 0.000 abstract 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 abstract 1
- MPMBRWOOISTHJV-XVNBXDOJSA-N [(e)-but-1-enyl]benzene Chemical compound CC\C=C\C1=CC=CC=C1 MPMBRWOOISTHJV-XVNBXDOJSA-N 0.000 abstract 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 1
- 150000002118 epoxides Chemical class 0.000 abstract 1
- 239000003822 epoxy resin Substances 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000004967 organic peroxy acids Chemical class 0.000 abstract 1
- 150000008379 phenol ethers Chemical class 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 abstract 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/28—Ethers with hydroxy compounds containing oxirane rings
-
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH886460X | 1959-07-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB886460A true GB886460A (en) | 1962-01-10 |
Family
ID=4545311
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB23698/60A Expired GB886460A (en) | 1959-07-06 | 1960-07-06 | Improvements in or relating to the manufacture of aromatic ethers |
Country Status (2)
| Country | Link |
|---|---|
| BE (1) | BE592617A (enrdf_load_stackoverflow) |
| GB (1) | GB886460A (enrdf_load_stackoverflow) |
-
0
- BE BE592617D patent/BE592617A/xx unknown
-
1960
- 1960-07-06 GB GB23698/60A patent/GB886460A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE592617A (enrdf_load_stackoverflow) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2951825A (en) | Glycidyl derivatives of amino phenols | |
| GB675168A (en) | Manufacture of epoxide resins | |
| GB675180A (en) | Improvements in epoxide compositions | |
| GB788556A (en) | Heat-curable resinous compositions containing glycidyl phenolic ethers and their method of manufacture | |
| GB875866A (en) | Improvements in and relating to epoxide compositions | |
| GB984633A (en) | Manufacture of epoxy resins | |
| US2865887A (en) | Glycidyl ethers of reaction products of certain phenols with polymerizable aromatic substances containing at least one vinyl group | |
| GB855205A (en) | Improvements in curing of polyepoxides | |
| GB1462536A (en) | Epoxy curing system | |
| GB886460A (en) | Improvements in or relating to the manufacture of aromatic ethers | |
| US3787508A (en) | Solid,curable polyepoxides modified with hydrolyzed liquid polyepoxides | |
| GB986204A (en) | Epoxy compounds and flame-retardant resins therefrom | |
| GB907341A (en) | Polyglycidyl ethers of polyphenols | |
| GB904403A (en) | Improvements in and relating to the curing of polyepoxides | |
| GB791303A (en) | Process for preparing compositions containing glycidyl ethers | |
| GB904549A (en) | Preparation of epoxy ethers and formation of cured resinous products therefrom | |
| US4663400A (en) | Epoxy resins prepared from trisphenols and dicyclopentadiene | |
| US3444111A (en) | Thermoset resins from an epoxy alcohol,a polyepoxide and cyclic anhydrides | |
| GB1008847A (en) | Thioether reaction products | |
| GB939210A (en) | Epoxy resin hardener compositions | |
| GB987015A (en) | Improvements in or relating to epoxide resins, processes for their production and their use | |
| GB907474A (en) | Epoxy-resins with high-quality electrical properties and a process for their manufacture | |
| GB887529A (en) | Hardenable compositions comprising epoxide compounds and boron trifluoride | |
| US3288761A (en) | Curable mistures of diepoxy compounds and dicarboxylic acid anhydrides | |
| GB859573A (en) | Improvements in resin compositions |