JPH0465817B2 - - Google Patents
Info
- Publication number
- JPH0465817B2 JPH0465817B2 JP58010489A JP1048983A JPH0465817B2 JP H0465817 B2 JPH0465817 B2 JP H0465817B2 JP 58010489 A JP58010489 A JP 58010489A JP 1048983 A JP1048983 A JP 1048983A JP H0465817 B2 JPH0465817 B2 JP H0465817B2
- Authority
- JP
- Japan
- Prior art keywords
- biphenyl
- compound
- group
- hydroxy
- acetoxy
- 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 - Lifetime
Links
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 49
- 235000010290 biphenyl Nutrition 0.000 claims description 32
- 239000004305 biphenyl Substances 0.000 claims description 32
- -1 biphenyl compound Chemical class 0.000 claims description 30
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims description 4
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 description 21
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 14
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 239000012279 sodium borohydride Substances 0.000 description 6
- 229910000033 sodium borohydride Inorganic materials 0.000 description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000000921 elemental analysis Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- QCZZSANNLWPGEA-UHFFFAOYSA-N 1-(4-phenylphenyl)ethanone Chemical group C1=CC(C(=O)C)=CC=C1C1=CC=CC=C1 QCZZSANNLWPGEA-UHFFFAOYSA-N 0.000 description 4
- DXXRWDCBHNIVBQ-UHFFFAOYSA-N 1-[4-(4-hydroxyphenyl)phenyl]ethanone Chemical group C1=CC(C(=O)C)=CC=C1C1=CC=C(O)C=C1 DXXRWDCBHNIVBQ-UHFFFAOYSA-N 0.000 description 4
- BWZNAPOWXNNKME-UHFFFAOYSA-N 4-(4-ethenylphenyl)phenol Chemical group C1=CC(O)=CC=C1C1=CC=C(C=C)C=C1 BWZNAPOWXNNKME-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 4
- 230000000397 acetylating effect Effects 0.000 description 4
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical group C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- GNHSLRMCJVPUAO-UHFFFAOYSA-N [4-(4-acetylphenyl)phenyl] acetate Chemical group C1=CC(OC(=O)C)=CC=C1C1=CC=C(C(C)=O)C=C1 GNHSLRMCJVPUAO-UHFFFAOYSA-N 0.000 description 3
- FTNWOKTUEOIFAN-UHFFFAOYSA-N [4-(4-ethenylphenyl)phenyl] acetate Chemical group C1=CC(OC(=O)C)=CC=C1C1=CC=C(C=C)C=C1 FTNWOKTUEOIFAN-UHFFFAOYSA-N 0.000 description 3
- 239000003905 agrochemical Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- KDCIHNCMPUBDKT-UHFFFAOYSA-N hexane;propan-2-one Chemical compound CC(C)=O.CCCCCC KDCIHNCMPUBDKT-UHFFFAOYSA-N 0.000 description 3
- 238000004811 liquid chromatography Methods 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- 239000011592 zinc chloride Substances 0.000 description 3
- 235000005074 zinc chloride Nutrition 0.000 description 3
- MISFQCBPASYYGV-UHFFFAOYSA-N (4-phenylphenyl) acetate Chemical group C1=CC(OC(=O)C)=CC=C1C1=CC=CC=C1 MISFQCBPASYYGV-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- WUPQNSSVDWETGF-UHFFFAOYSA-N [4-[4-(1-hydroxyethyl)phenyl]phenyl] acetate Chemical group C1=CC(C(O)C)=CC=C1C1=CC=C(OC(C)=O)C=C1 WUPQNSSVDWETGF-UHFFFAOYSA-N 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 125000006267 biphenyl group Chemical group 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000012280 lithium aluminium hydride Substances 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 2
- UZUGIHHGLRFGMJ-UHFFFAOYSA-N (2-phenylphenyl) acetate Chemical group CC(=O)OC1=CC=CC=C1C1=CC=CC=C1 UZUGIHHGLRFGMJ-UHFFFAOYSA-N 0.000 description 1
- XIRPMPKSZHNMST-UHFFFAOYSA-N 1-ethenyl-2-phenylbenzene Chemical group C=CC1=CC=CC=C1C1=CC=CC=C1 XIRPMPKSZHNMST-UHFFFAOYSA-N 0.000 description 1
- WKJXRESRYVFQIY-UHFFFAOYSA-N 4-[4-(1-hydroxyethyl)phenyl]phenol Chemical group C1=CC(C(O)C)=CC=C1C1=CC=C(O)C=C1 WKJXRESRYVFQIY-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 229920001002 functional polymer Polymers 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000006462 rearrangement reaction Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1048983A JPS59137433A (ja) | 1983-01-27 | 1983-01-27 | 新規ビフエニル化合物 |
| US06/569,667 US4670581A (en) | 1983-01-27 | 1984-01-10 | Biphenyl compounds and process for producing the same |
| GB08400723A GB2137982B (en) | 1983-01-27 | 1984-01-12 | New biphenyl compounds and process for producing the same |
| NL8400220A NL190719C (nl) | 1983-01-27 | 1984-01-24 | Bifenylderivaten. |
| FR848401259A FR2542733B1 (fr) | 1983-01-27 | 1984-01-27 | Nouveaux derives de biphenyle et leur preparation |
| DE19843402831 DE3402831A1 (de) | 1983-01-27 | 1984-01-27 | Neue biphenylverbindungen und verfahren zu deren herstellung |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1048983A JPS59137433A (ja) | 1983-01-27 | 1983-01-27 | 新規ビフエニル化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59137433A JPS59137433A (ja) | 1984-08-07 |
| JPH0465817B2 true JPH0465817B2 (ko) | 1992-10-21 |
Family
ID=11751583
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1048983A Granted JPS59137433A (ja) | 1983-01-27 | 1983-01-27 | 新規ビフエニル化合物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59137433A (ko) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4569352B2 (ja) * | 2005-03-30 | 2010-10-27 | 住友化学株式会社 | エポキシ化合物およびエポキシ樹脂硬化物 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5025537A (ko) * | 1973-06-01 | 1975-03-18 | ||
| JPS57301A (en) * | 1980-06-03 | 1982-01-05 | Susumu Mitoya | Prime mover with internal power |
-
1983
- 1983-01-27 JP JP1048983A patent/JPS59137433A/ja active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5025537A (ko) * | 1973-06-01 | 1975-03-18 | ||
| JPS57301A (en) * | 1980-06-03 | 1982-01-05 | Susumu Mitoya | Prime mover with internal power |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4569352B2 (ja) * | 2005-03-30 | 2010-10-27 | 住友化学株式会社 | エポキシ化合物およびエポキシ樹脂硬化物 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59137433A (ja) | 1984-08-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU1223842A3 (ru) | Способ получени производных бензофенонгидразонов | |
| CN109970755B (zh) | 取代的水杨醛衍生物的合成 | |
| JPH0481975B2 (ko) | ||
| JPS6212772B2 (ko) | ||
| JPH0465817B2 (ko) | ||
| JPS6148830B2 (ko) | ||
| CN115583902B (zh) | 一种炔基硫醚类化合物的制备方法 | |
| JP3912758B2 (ja) | １，１−ジ置換−１Ｈ−ベンゾ〔ｅ〕インドール化合物の製造方法及び４〜９位ヒドロキシ基置換の該化合物 | |
| EP0047674A1 (en) | Novel process for preparing isoindolin derivatives | |
| JP2564141B2 (ja) | アルキルベンゾチアゾール類の製造方法 | |
| JP4759722B2 (ja) | 置換基を有する芳香族カルボン酸エステルの製造方法 | |
| JPS6226260A (ja) | ７，７，８，８−テトラシアノキノジメタン−２，５−イレン−（３−プロピオン酸）類およびその製造法 | |
| JPS621651B2 (ko) | ||
| JP2706554B2 (ja) | ４―トリフルオロメチルアニリン誘導体及びその製造法 | |
| JPH01186852A (ja) | アミド基含有ジフェニルジアセチレン | |
| JPS5913513B2 (ja) | シンキシツフエンキカゴウブツ ノ セイゾウホウ | |
| JPH07247267A (ja) | フェニルエーテル類の製造方法 | |
| SU1318593A1 (ru) | Способ получени алкилпроизводных хинолина | |
| CN115108932A (zh) | 一种芳香酰胺类化合物的制备方法 | |
| JPS62258351A (ja) | テトラエチルウレアの製造方法 | |
| JPH0583537B2 (ko) | ||
| JPH09227485A (ja) | ２−ヒドラジノナフタレン化合物の製造方法 | |
| JPS61129147A (ja) | マンデル酸およびその誘導体の製造方法 | |
| JPS60112731A (ja) | 新規ビフェニル化合物 | |
| JPH0920782A (ja) | ベンゾビスオキサゾロン誘導体の製造法及びその中間体 |