BE568181A - - Google Patents
Info
- Publication number
- BE568181A BE568181A BE568181DA BE568181A BE 568181 A BE568181 A BE 568181A BE 568181D A BE568181D A BE 568181DA BE 568181 A BE568181 A BE 568181A
- Authority
- BE
- Belgium
- Prior art keywords
- acetal
- cyclo
- reaction
- alcohol
- groups
- Prior art date
Links
- 238000000034 method Methods 0.000 claims description 57
- 150000001241 acetals Chemical class 0.000 claims description 49
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 45
- 238000006243 chemical reaction Methods 0.000 claims description 32
- 239000000835 fiber Substances 0.000 claims description 28
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 26
- 239000000047 product Substances 0.000 claims description 24
- 125000001931 aliphatic group Chemical group 0.000 claims description 19
- 238000002360 preparation method Methods 0.000 claims description 14
- 239000011541 reaction mixture Substances 0.000 claims description 14
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 13
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 claims description 11
- 150000001298 alcohols Chemical class 0.000 claims description 10
- 125000004036 acetal group Chemical group 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 8
- 150000001721 carbon Chemical group 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- -1 tetra (hydroxymethyl) dodecane Chemical compound 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000007859 condensation product Substances 0.000 claims 3
- 239000000470 constituent Substances 0.000 claims 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 235000019441 ethanol Nutrition 0.000 description 30
- 238000002844 melting Methods 0.000 description 24
- 230000008018 melting Effects 0.000 description 24
- 229920000642 polymer Polymers 0.000 description 22
- 238000001816 cooling Methods 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 13
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
- 238000009833 condensation Methods 0.000 description 12
- 230000005494 condensation Effects 0.000 description 12
- 239000000203 mixture Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 238000006482 condensation reaction Methods 0.000 description 8
- 239000003153 chemical reaction reagent Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 description 6
- 239000001569 carbon dioxide Substances 0.000 description 6
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- FGXADKJCJXPPIK-UHFFFAOYSA-N 1,1,8,8-tetraethoxyoctane Chemical compound CCOC(OCC)CCCCCCC(OCC)OCC FGXADKJCJXPPIK-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- 229920006324 polyoxymethylene Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- KRSOWIJSDPLQTH-UHFFFAOYSA-N 2,9-bis(hydroxymethyl)decane-1,10-diol Chemical compound OCC(CO)CCCCCCC(CO)CO KRSOWIJSDPLQTH-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000008259 solid foam Substances 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- JIQDXKKXHABQMX-UHFFFAOYSA-N 1,1,5,5-tetraethoxypentane Chemical compound CCOC(OCC)CCCC(OCC)OCC JIQDXKKXHABQMX-UHFFFAOYSA-N 0.000 description 2
- OTAIXAVNCGHMKV-UHFFFAOYSA-N 1,1,6,6-tetraethoxyhexane Chemical compound CCOC(OCC)CCCCC(OCC)OCC OTAIXAVNCGHMKV-UHFFFAOYSA-N 0.000 description 2
- YEJAJAKMYXTSRJ-UHFFFAOYSA-N 1,1,7,7-tetraethoxyheptane Chemical compound CCOC(OCC)CCCCCC(OCC)OCC YEJAJAKMYXTSRJ-UHFFFAOYSA-N 0.000 description 2
- TXGHOSDIGLWWFE-UHFFFAOYSA-N 1,1,8,8-tetramethoxyoctane Chemical compound COC(OC)CCCCCCC(OC)OC TXGHOSDIGLWWFE-UHFFFAOYSA-N 0.000 description 2
- VDMXPMYSWFDBJB-UHFFFAOYSA-N 1-ethoxypentane Chemical compound CCCCCOCC VDMXPMYSWFDBJB-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- NAWDYYCJZKMYLT-UHFFFAOYSA-N C(C)OC(CCCCCCCCCCC(OCC)OCC)OCC Chemical compound C(C)OC(CCCCCCCCCCC(OCC)OCC)OCC NAWDYYCJZKMYLT-UHFFFAOYSA-N 0.000 description 2
- 229930182556 Polyacetal Natural products 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- OYCGESINDSOZTG-UHFFFAOYSA-N 1,10-dibromododecane Chemical compound CCC(Br)CCCCCCCCCBr OYCGESINDSOZTG-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- ULTHEAFYOOPTTB-UHFFFAOYSA-N 1,4-dibromobutane Chemical compound BrCCCCBr ULTHEAFYOOPTTB-UHFFFAOYSA-N 0.000 description 1
- LOLANUHFGPZTLQ-UHFFFAOYSA-N 1-ethoxydecane Chemical compound CCCCCCCCCCOCC LOLANUHFGPZTLQ-UHFFFAOYSA-N 0.000 description 1
- HAOXTAJLDMZCQJ-UHFFFAOYSA-N 1-ethoxydodecane Chemical compound CCCCCCCCCCCCOCC HAOXTAJLDMZCQJ-UHFFFAOYSA-N 0.000 description 1
- 208000001840 Dandruff Diseases 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- OILAIQUEIWYQPH-UHFFFAOYSA-N cyclohexane-1,2-dione Chemical compound O=C1CCCCC1=O OILAIQUEIWYQPH-UHFFFAOYSA-N 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- UKFXDFUAPNAMPJ-UHFFFAOYSA-N ethylmalonic acid Chemical compound CCC(C(O)=O)C(O)=O UKFXDFUAPNAMPJ-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 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
- C08G4/00—Condensation polymers of aldehydes or ketones with polyalcohols; Addition polymers of heterocyclic oxygen compounds containing in the ring at least once the grouping —O—C—O—
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Artificial Filaments (AREA)
- Polyethers (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE568181A true BE568181A (en:Method) |
Family
ID=187619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE568181D BE568181A (en:Method) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE568181A (en:Method) |
-
0
- BE BE568181D patent/BE568181A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2729516B1 (fr) | Nouveau polyamide, procede de preparation et utilisations | |
| KR20120106997A (ko) | 폴리다이오르가노실록산 폴리옥사미드 공중합체의 제조 방법 | |
| EP2931760A1 (fr) | Polymères hydrocarbonés comportant deux groupements terminaux à terminaisons 2-oxo-1,3-dioxolan-4-yl, leur préparation et leur utilisation | |
| CA1133187A (fr) | Copolyesters alcoylaromatiques thermotropes | |
| WO2012136942A1 (fr) | Procede de fabrication de polycarbonate a partir de dialkylcarbonate de dianhydrohexitol | |
| EP3673003B1 (fr) | Polymeres multiblocs dont la synthese met en oeuvre d'oligocarbonates polyols | |
| BE568181A (en:Method) | ||
| EP0026720B1 (fr) | Masses fondues anisotropes conformables à base de polyesters aromatiques, leurs procédés de préparation et articles formés à partir d'elles | |
| EP3938356B1 (fr) | Procede de fabrication d'un monomere polybenzoxazine | |
| EP0680465B1 (fr) | Procede de preparation d'un monoamide alpha-amino omega-ester | |
| CN119325488A (zh) | 含硫高分子化合物及其制备方法、聚合物组合物以及含硫化合物 | |
| US3923750A (en) | Process for preparing wholly aromatic polyamides in the presence of an aryl sulfone | |
| CH616693A5 (en:Method) | ||
| EP0220080A1 (fr) | Compositions d'oligomères de polyaryloxypyridine à terminaisons phtalonitriles, leur préparation, leur utilisation dans la fabrication de réseaux de polyaryloxypyridine copolyphtalocyanines, et les réseaux obtenus | |
| EP3938357B1 (fr) | Procede de fabrication d'un monomere polybenzoxazine | |
| WO2023118667A1 (en) | Sulfur-bridged thermoplastic polyesters and thermosets from furfural | |
| BE430373A (en:Method) | ||
| BE560045A (en:Method) | ||
| BE463298A (en:Method) | ||
| FR2691150A1 (fr) | Triéthylnylborazines, leur préparation et leur utilisation notamment pour la préparation de céramique essentiellement à base de nitrure de bore. | |
| WO1993018086A1 (fr) | Copolymere polyester/polydiorganosiloxane, composition contenant ce polymere et procedes de fabrication de ce copolymere et cette composition | |
| FR2854894A1 (fr) | 2-nitratoethyloxirane, poly(2-nitratoethyloxirane) et leur procede de preparation | |
| FR3112782A1 (fr) | Procede de polymerisation de chromenes par voie cationique | |
| CN119912668A (zh) | 线性脂肪族聚酯的合成 | |
| BE594260A (en:Method) |