JPS6126900B2 - - Google Patents
Info
- Publication number
- JPS6126900B2 JPS6126900B2 JP14550878A JP14550878A JPS6126900B2 JP S6126900 B2 JPS6126900 B2 JP S6126900B2 JP 14550878 A JP14550878 A JP 14550878A JP 14550878 A JP14550878 A JP 14550878A JP S6126900 B2 JPS6126900 B2 JP S6126900B2
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- trans
- phthalonitrile
- compound
- butoxy
- 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
- 239000004973 liquid crystal related substance Substances 0.000 claims description 49
- 229920006391 phthalonitrile polymer Polymers 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 12
- MPAIWVOBMLSHQA-UHFFFAOYSA-N 3,6-dihydroxybenzene-1,2-dicarbonitrile Chemical compound OC1=CC=C(O)C(C#N)=C1C#N MPAIWVOBMLSHQA-UHFFFAOYSA-N 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- PFJVIOBMBDFBCJ-UHFFFAOYSA-N (1z)-1-diazobutane Chemical compound CCCC=[N+]=[N-] PFJVIOBMBDFBCJ-UHFFFAOYSA-N 0.000 claims description 3
- 150000004820 halides Chemical class 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims description 2
- 238000013329 compounding Methods 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 31
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 239000000463 material Substances 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 8
- 150000002148 esters Chemical class 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical compound N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 3
- ZEYHEAKUIGZSGI-UHFFFAOYSA-N 4-methoxybenzoic acid Chemical compound COC1=CC=C(C(O)=O)C=C1 ZEYHEAKUIGZSGI-UHFFFAOYSA-N 0.000 description 3
- 239000004990 Smectic liquid crystal Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- FEIWNULTQYHCDN-UHFFFAOYSA-N mbba Chemical compound C1=CC(CCCC)=CC=C1N=CC1=CC=C(OC)C=C1 FEIWNULTQYHCDN-UHFFFAOYSA-N 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- HBQUXMZZODHFMJ-UHFFFAOYSA-N 4-hexoxybenzoic acid Chemical compound CCCCCCOC1=CC=C(C(O)=O)C=C1 HBQUXMZZODHFMJ-UHFFFAOYSA-N 0.000 description 2
- QYJXDIUNDMRLAO-UHFFFAOYSA-N butyl 4-methylbenzenesulfonate Chemical compound CCCCOS(=O)(=O)C1=CC=C(C)C=C1 QYJXDIUNDMRLAO-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- NZNMSOFKMUBTKW-UHFFFAOYSA-N cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- KMVXENDYYJFUGZ-UHFFFAOYSA-N n-methoxy-n-(5-phenylpent-4-enyl)aniline Chemical compound C=1C=CC=CC=1N(OC)CCCC=CC1=CC=CC=C1 KMVXENDYYJFUGZ-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- -1 trans-p-butylcyclohexynecarboxylic acid Chemical compound 0.000 description 2
- PESGGHASCQJIRP-UHFFFAOYSA-N (2-butylphenyl)imino-oxido-phenylazanium Chemical compound C(CCC)C1=C(C=CC=C1)N=[N+]([O-])C1=CC=CC=C1 PESGGHASCQJIRP-UHFFFAOYSA-N 0.000 description 1
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 description 1
- BALGERHMIXFENA-UHFFFAOYSA-N 4-butylcyclohexane-1-carboxylic acid Chemical compound CCCCC1CCC(C(O)=O)CC1 BALGERHMIXFENA-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- RVLAXPQGTRTHEV-XYPYZODXSA-N CCCCC[C@H]1CC[C@H](C(O)=O)CC1 Chemical compound CCCCC[C@H]1CC[C@H](C(O)=O)CC1 RVLAXPQGTRTHEV-XYPYZODXSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- WZWRHKQSYZLFDM-UHFFFAOYSA-N N-ethoxy-N-(5-phenylpent-4-enyl)aniline Chemical compound C(C)ON(C1=CC=CC=C1)CCCC=CC1=CC=CC=C1 WZWRHKQSYZLFDM-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- GAUZCKBSTZFWCT-UHFFFAOYSA-N azoxybenzene Chemical compound C=1C=CC=CC=1[N+]([O-])=NC1=CC=CC=C1 GAUZCKBSTZFWCT-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- DBOAVDSSZWDGTH-UHFFFAOYSA-N n-(4-butylphenyl)-1-(4-ethoxyphenyl)methanimine Chemical compound C1=CC(CCCC)=CC=C1N=CC1=CC=C(OCC)C=C1 DBOAVDSSZWDGTH-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical class C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14550878A JPS5572156A (en) | 1978-11-25 | 1978-11-25 | 3-butoxy-6-cyclohexanecarboxy-phthalonitriles |
| US06/074,655 US4279770A (en) | 1978-09-20 | 1979-09-12 | Liquid crystal 2,3-dicyano-hydroquinone derivatives |
| DE2937700A DE2937700C2 (de) | 1978-09-20 | 1979-09-18 | 2,3-Dicyano-hydrochinon-Derivate und Flüssigkristallmaterialien, die diese Derivate enthalten |
| CA335,840A CA1131655A (en) | 1978-09-20 | 1979-09-18 | 2,3-dicyano-hydroquinone derivatives |
| CH845579A CH642345A5 (de) | 1978-09-20 | 1979-09-19 | 2,3-dicyano-hydrochinon derivate. |
| GB7932598A GB2035303B (en) | 1978-09-20 | 1979-09-20 | 2,3-dicyano-hydroquinone derivatives |
| FR7923469A FR2436777A1 (fr) | 1978-09-20 | 1979-09-20 | Derive de la 2,3-dicyano-hydroquinone et leur application aux liquides |
| DD79215670A DD146187A5 (de) | 1978-09-20 | 1979-09-20 | Verfahren zur herstellung von 2-chlor-6-nitroanilinen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14550878A JPS5572156A (en) | 1978-11-25 | 1978-11-25 | 3-butoxy-6-cyclohexanecarboxy-phthalonitriles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5572156A JPS5572156A (en) | 1980-05-30 |
| JPS6126900B2 true JPS6126900B2 (hu) | 1986-06-23 |
Family
ID=15386864
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14550878A Granted JPS5572156A (en) | 1978-09-20 | 1978-11-25 | 3-butoxy-6-cyclohexanecarboxy-phthalonitriles |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5572156A (hu) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5734176A (en) * | 1980-08-08 | 1982-02-24 | Hitachi Ltd | Liquid crystal composition |
| JP4789502B2 (ja) * | 2005-04-26 | 2011-10-12 | 東京電力株式会社 | 電位差法を用いた深い亀裂に対する亀裂深さ測定手法および装置 |
-
1978
- 1978-11-25 JP JP14550878A patent/JPS5572156A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5572156A (en) | 1980-05-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1131655A (en) | 2,3-dicyano-hydroquinone derivatives | |
| JPS6054341A (ja) | 液晶性炭酸エステル類 | |
| JPH0623135B2 (ja) | 液晶物質及び液晶組成物 | |
| EP0268198A2 (de) | Ferroelektrische Flüssigkristalle | |
| EP0162437B1 (en) | Liquid crystal compound and liquid crystal composition including the same | |
| JPS6126899B2 (hu) | ||
| JPS6126900B2 (hu) | ||
| EP1470105B1 (en) | Liquid crystal compounds | |
| JPH06256339A (ja) | クロマン誘導体 | |
| JPH0717905B2 (ja) | 液晶組成物 | |
| JPS6126898B2 (hu) | ||
| JPS6123784B2 (hu) | ||
| JPS6312056B2 (hu) | ||
| JPS6126901B2 (hu) | ||
| JPS6312057B2 (hu) | ||
| JP2862266B2 (ja) | カルボン酸エステル化合物および液晶化合物 | |
| JP2745073B2 (ja) | フェニルアセチレン化合物 | |
| JPS5959648A (ja) | 液晶性化合物 | |
| JP2925682B2 (ja) | 新規なエステル化合物、これを含む液晶組成物及び光スイッチング素子 | |
| JP2907993B2 (ja) | 液晶組成物およびその用途 | |
| JP2901695B2 (ja) | 液晶組成物およびその用途 | |
| JP2786513B2 (ja) | エステル化合物及びこれを含む液晶組成物 | |
| JP2919930B2 (ja) | カルボン酸エステル化合物および液晶化合物 | |
| JPS5910557A (ja) | ３−アルキルオキシ−６−ヒドロキシ−フタロニトリルのトランス−４−（トランス−４′−アルキルシクロヘキシル）シクロヘキサンカルボン酸エステル類 | |
| JP2862894B2 (ja) | 液晶組成物およびその用途 |