DD231361A1 - Verfahren zur herstellung monomerer li-addukte an konjugierte diene - Google Patents
Verfahren zur herstellung monomerer li-addukte an konjugierte diene Download PDFInfo
- Publication number
- DD231361A1 DD231361A1 DD24163382A DD24163382A DD231361A1 DD 231361 A1 DD231361 A1 DD 231361A1 DD 24163382 A DD24163382 A DD 24163382A DD 24163382 A DD24163382 A DD 24163382A DD 231361 A1 DD231361 A1 DD 231361A1
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- diene
- adducts
- lithium
- aromatic compound
- polycyclic aromatic
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title abstract description 4
- 150000001993 dienes Chemical class 0.000 claims abstract description 16
- 239000011541 reaction mixture Substances 0.000 claims abstract description 12
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims abstract description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 11
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000006243 chemical reaction Methods 0.000 claims abstract description 10
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 10
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 8
- -1 polycyclic aromatic compound Chemical class 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000002244 precipitate Substances 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 3
- 150000002641 lithium Chemical class 0.000 abstract 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 34
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 8
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 6
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 239000007791 liquid phase Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 125000002524 organometallic group Chemical group 0.000 description 3
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 2
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241001314535 Ophrys apifera Species 0.000 description 1
- QSNQXZYQEIKDPU-UHFFFAOYSA-N [Li].[Fe] Chemical compound [Li].[Fe] QSNQXZYQEIKDPU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- VLLYOYVKQDKAHN-UHFFFAOYSA-N buta-1,3-diene;2-methylbuta-1,3-diene Chemical compound C=CC=C.CC(=C)C=C VLLYOYVKQDKAHN-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- SMBQBQBNOXIFSF-UHFFFAOYSA-N dilithium Chemical compound [Li][Li] SMBQBQBNOXIFSF-UHFFFAOYSA-N 0.000 description 1
- 238000002079 electron magnetic resonance spectroscopy Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000005051 trimethylchlorosilane Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS559981A CS229066B1 (en) | 1981-07-22 | 1981-07-22 | Method of preparing monomeric lithium adducts anto conjugated dienes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD231361A1 true DD231361A1 (de) | 1985-12-24 |
Family
ID=5401165
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD24163382A DD231361A1 (de) | 1981-07-22 | 1982-07-14 | Verfahren zur herstellung monomerer li-addukte an konjugierte diene |
Country Status (2)
| Country | Link |
|---|---|
| CS (1) | CS229066B1 (cs) |
| DD (1) | DD231361A1 (cs) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019038099A1 (en) | 2017-08-24 | 2019-02-28 | Total Research & Technology Feluy | POLYLACTIDE-BASED COMPOSITIONS |
| WO2019038098A1 (en) | 2017-08-24 | 2019-02-28 | Total Research & Technology Feluy | POLYLACTIDE-BASED COMPOSITIONS |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20220033627A1 (en) | 2020-07-29 | 2022-02-03 | Fina Technology, Inc. | Silane modified styrene butadiene copolymer for high performance in dry adherence, wet adherence and rolling resistance |
-
1981
- 1981-07-22 CS CS559981A patent/CS229066B1/cs unknown
-
1982
- 1982-07-14 DD DD24163382A patent/DD231361A1/de not_active IP Right Cessation
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019038099A1 (en) | 2017-08-24 | 2019-02-28 | Total Research & Technology Feluy | POLYLACTIDE-BASED COMPOSITIONS |
| WO2019038098A1 (en) | 2017-08-24 | 2019-02-28 | Total Research & Technology Feluy | POLYLACTIDE-BASED COMPOSITIONS |
Also Published As
| Publication number | Publication date |
|---|---|
| CS229066B1 (en) | 1984-05-14 |
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| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |