JPS5850977B2 - タンサンジアリ−ルノセイゾウホウホウ - Google Patents
タンサンジアリ−ルノセイゾウホウホウInfo
- Publication number
- JPS5850977B2 JPS5850977B2 JP50118315A JP11831575A JPS5850977B2 JP S5850977 B2 JPS5850977 B2 JP S5850977B2 JP 50118315 A JP50118315 A JP 50118315A JP 11831575 A JP11831575 A JP 11831575A JP S5850977 B2 JPS5850977 B2 JP S5850977B2
- Authority
- JP
- Japan
- Prior art keywords
- phosgene
- reaction
- phenol
- catalyst
- aromatic
- 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
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 31
- 238000006243 chemical reaction Methods 0.000 claims description 25
- -1 diaryl carbonate Chemical compound 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 229910017464 nitrogen compound Inorganic materials 0.000 claims description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 10
- 150000002830 nitrogen compounds Chemical class 0.000 claims description 10
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 9
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 8
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 7
- 230000003197 catalytic effect Effects 0.000 claims description 7
- 230000008030 elimination Effects 0.000 claims description 5
- 238000003379 elimination reaction Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 238000000034 method Methods 0.000 description 27
- 239000003054 catalyst Substances 0.000 description 24
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 21
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 21
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 13
- 239000011541 reaction mixture Substances 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- YQUQWHNMBPIWGK-UHFFFAOYSA-N 4-isopropylphenol Chemical compound CC(C)C1=CC=C(O)C=C1 YQUQWHNMBPIWGK-UHFFFAOYSA-N 0.000 description 4
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 4
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 4
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 4
- AHWALFGBDFAJAI-UHFFFAOYSA-N phenyl carbonochloridate Chemical compound ClC(=O)OC1=CC=CC=C1 AHWALFGBDFAJAI-UHFFFAOYSA-N 0.000 description 4
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000002837 carbocyclic group Chemical group 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000012458 free base Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- UMHSKYSHOIGDPE-UHFFFAOYSA-N pyridine;quinoline Chemical compound C1=CC=NC=C1.N1=CC=CC2=CC=CC=C21 UMHSKYSHOIGDPE-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- ZLWULWWXACZTPR-UHFFFAOYSA-N [ClH]=O Chemical class [ClH]=O ZLWULWWXACZTPR-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 150000001556 benzimidazoles Chemical class 0.000 description 2
- 150000001565 benzotriazoles Chemical class 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229910052736 halogen Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002391 heterocyclic compounds Chemical class 0.000 description 2
- 150000003840 hydrochlorides Chemical class 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- ZXPCCXXSNUIVNK-UHFFFAOYSA-N 1,1,1,2,3-pentachloropropane Chemical compound ClCC(Cl)C(Cl)(Cl)Cl ZXPCCXXSNUIVNK-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- JBGNINOUZCHFPB-UHFFFAOYSA-N 2,4,6-trimethyl-1h-triazine Chemical compound CN1NC(C)=CC(C)=N1 JBGNINOUZCHFPB-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- AGIJRRREJXSQJR-UHFFFAOYSA-N 2h-thiazine Chemical compound N1SC=CC=C1 AGIJRRREJXSQJR-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- GCNTZFIIOFTKIY-UHFFFAOYSA-N 4-hydroxypyridine Chemical compound OC1=CC=NC=C1 GCNTZFIIOFTKIY-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 238000003436 Schotten-Baumann reaction Methods 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001341 alkaline earth metal compounds Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- LBKPGNUOUPTQKA-UHFFFAOYSA-N ethyl n-phenylcarbamate Chemical class CCOC(=O)NC1=CC=CC=C1 LBKPGNUOUPTQKA-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- SIAPCJWMELPYOE-UHFFFAOYSA-N lithium hydride Chemical compound [LiH] SIAPCJWMELPYOE-UHFFFAOYSA-N 0.000 description 1
- 229910000103 lithium hydride Inorganic materials 0.000 description 1
- 125000003717 m-cresyl group Chemical group [H]C1=C([H])C(O*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-methyl-PhOH Natural products CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- XLSZMDLNRCVEIJ-UHFFFAOYSA-N methylimidazole Natural products CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000004893 oxazines Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical class OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- LBFSHXXTLRZXST-UHFFFAOYSA-N pyridazine;pyrimidine Chemical compound C1=CC=NN=C1.C1=CN=CN=C1 LBFSHXXTLRZXST-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 150000004897 thiazines Chemical class 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/02—Preparation of esters of carbonic or haloformic acids from phosgene or haloformates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2447348A DE2447348C2 (de) | 1974-10-04 | 1974-10-04 | Verfahren zur Herstellung von Diarylcarbonaten |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5163148A JPS5163148A (en) | 1976-06-01 |
| JPS5850977B2 true JPS5850977B2 (ja) | 1983-11-14 |
Family
ID=5927512
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50118315A Expired JPS5850977B2 (ja) | 1974-10-04 | 1975-10-02 | タンサンジアリ−ルノセイゾウホウホウ |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4012406A (enExample) |
| JP (1) | JPS5850977B2 (enExample) |
| BE (1) | BE834167A (enExample) |
| BR (1) | BR7506452A (enExample) |
| CA (1) | CA1042912A (enExample) |
| DE (1) | DE2447348C2 (enExample) |
| DK (1) | DK447375A (enExample) |
| FR (1) | FR2286810A1 (enExample) |
| GB (1) | GB1498713A (enExample) |
| IL (1) | IL48213A0 (enExample) |
| IT (1) | IT1047665B (enExample) |
| LU (1) | LU73499A1 (enExample) |
| NL (1) | NL7511678A (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62197384U (enExample) * | 1987-04-23 | 1987-12-15 | ||
| JPH115767A (ja) * | 1997-06-16 | 1999-01-12 | Mitsubishi Chem Corp | ジアリールカーボネートの精製方法 |
| JPH115766A (ja) * | 1997-06-16 | 1999-01-12 | Mitsubishi Chem Corp | ジアリールカーボネートの製造方法 |
| JPH1129532A (ja) * | 1997-07-08 | 1999-02-02 | Mitsubishi Chem Corp | ジアリールカーボネートの精製方法 |
| JP2006144023A (ja) * | 1999-12-28 | 2006-06-08 | Mitsubishi Chemicals Corp | 一酸化炭素の製造方法、ホスゲンの製造方法及び炭酸ジアリールの製造方法 |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4365055A (en) * | 1981-06-24 | 1982-12-21 | Ppg Industries, Inc. | Process for producing substantially linear carbonate polymer |
| US4697034A (en) * | 1985-11-15 | 1987-09-29 | General Electric Company | Process for making diaryl carbonates |
| US5183919A (en) * | 1989-12-18 | 1993-02-02 | The Dow Chemical Company | Process for the preparation of diaryl carbonates |
| US5136077A (en) * | 1989-12-18 | 1992-08-04 | The Dow Chemical Company | Process for the preparation of diaryl carbonates |
| US5167946A (en) * | 1990-12-27 | 1992-12-01 | The Dow Chemical Company | Diaryl carbonate process |
| US5380909A (en) * | 1991-06-24 | 1995-01-10 | The Dow Chemical Company | Captive carbonyl halide process for production of diaryl carbonates |
| US6175017B1 (en) | 1991-10-22 | 2001-01-16 | Bayer Aktiengesellschaft | Process for the production of aryl carbonates |
| US5731453A (en) * | 1996-03-12 | 1998-03-24 | Ube Industries, Ltd. | Process for producing a diaryl carbonate |
| US5922827A (en) * | 1996-09-27 | 1999-07-13 | Ube Industries, Ltd. | Process for producing a polycarbonate |
| US5834615A (en) * | 1996-09-27 | 1998-11-10 | Ube Industries, Ltd. | Process for producing diaryl carbonate |
| DE60042195D1 (de) * | 1999-12-28 | 2009-06-25 | Mitsubishi Chem Corp | Verfahren zum Herstellen von Diarylcarbonat |
| US7151189B2 (en) | 2003-06-19 | 2006-12-19 | General Electric Company | Method and apparatus for waste stream recovery |
| US9175135B2 (en) | 2010-03-30 | 2015-11-03 | Bayer Materialscience Ag | Process for preparing diaryl carbonates and polycarbonates |
| JP6352175B2 (ja) * | 2011-07-08 | 2018-07-04 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ | ジアリールカーボネートの製造方法 |
| WO2014095776A1 (de) | 2012-12-18 | 2014-06-26 | Bayer Materialscience Ag | Verfahren zur herstellung von diarylcarbonat |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2837555A (en) * | 1956-09-20 | 1958-06-03 | Dow Chemical Co | Preparation of carbonate esters |
| US3170946A (en) * | 1961-08-17 | 1965-02-23 | Union Carbide Corp | Preparation of arylchloroformates |
| US3211776A (en) * | 1963-01-22 | 1965-10-12 | Du Pont | Catalytic process for preparing aromatic chloroformates |
| US3211775A (en) * | 1963-01-22 | 1965-10-12 | Du Pont | Catalytic process for preparing aromatic chloroformates |
| US3211774A (en) * | 1963-01-22 | 1965-10-12 | Du Pont | Process for preparing aromatic esters of chloroformic acid |
-
1974
- 1974-10-04 DE DE2447348A patent/DE2447348C2/de not_active Expired
-
1975
- 1975-09-30 IL IL48213A patent/IL48213A0/xx unknown
- 1975-09-30 US US05/618,057 patent/US4012406A/en not_active Expired - Lifetime
- 1975-10-01 GB GB40122/75A patent/GB1498713A/en not_active Expired
- 1975-10-02 LU LU73499A patent/LU73499A1/xx unknown
- 1975-10-02 CA CA236,906A patent/CA1042912A/en not_active Expired
- 1975-10-02 IT IT51609/75A patent/IT1047665B/it active
- 1975-10-02 JP JP50118315A patent/JPS5850977B2/ja not_active Expired
- 1975-10-03 DK DK447375A patent/DK447375A/da unknown
- 1975-10-03 BE BE160664A patent/BE834167A/xx unknown
- 1975-10-03 FR FR7530411A patent/FR2286810A1/fr active Granted
- 1975-10-03 BR BR7506452*A patent/BR7506452A/pt unknown
- 1975-10-03 NL NL7511678A patent/NL7511678A/xx unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62197384U (enExample) * | 1987-04-23 | 1987-12-15 | ||
| JPH115767A (ja) * | 1997-06-16 | 1999-01-12 | Mitsubishi Chem Corp | ジアリールカーボネートの精製方法 |
| JPH115766A (ja) * | 1997-06-16 | 1999-01-12 | Mitsubishi Chem Corp | ジアリールカーボネートの製造方法 |
| JPH1129532A (ja) * | 1997-07-08 | 1999-02-02 | Mitsubishi Chem Corp | ジアリールカーボネートの精製方法 |
| JP2006144023A (ja) * | 1999-12-28 | 2006-06-08 | Mitsubishi Chemicals Corp | 一酸化炭素の製造方法、ホスゲンの製造方法及び炭酸ジアリールの製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2447348A1 (de) | 1976-04-15 |
| US4012406A (en) | 1977-03-15 |
| LU73499A1 (enExample) | 1976-08-19 |
| BE834167A (fr) | 1976-04-05 |
| CA1042912A (en) | 1978-11-21 |
| NL7511678A (nl) | 1976-04-06 |
| DE2447348C2 (de) | 1983-11-10 |
| BR7506452A (pt) | 1976-08-10 |
| FR2286810B1 (enExample) | 1980-02-08 |
| FR2286810A1 (fr) | 1976-04-30 |
| DK447375A (da) | 1976-04-05 |
| IL48213A0 (en) | 1975-11-25 |
| JPS5163148A (en) | 1976-06-01 |
| GB1498713A (en) | 1978-01-25 |
| IT1047665B (it) | 1980-10-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS5850977B2 (ja) | タンサンジアリ−ルノセイゾウホウホウ | |
| US6469192B1 (en) | Solventless preparation of ester-substituted diaryl carbonates | |
| US4261922A (en) | Process for alkoxylation of phenols | |
| US4360686A (en) | Silylation of organic compounds | |
| CN101084179A (zh) | 制备碳酸二烷基酯的方法 | |
| US3234263A (en) | Process for preparing diaryl carbonates | |
| US3170946A (en) | Preparation of arylchloroformates | |
| JP3071008B2 (ja) | アリールカーボネートの製法 | |
| US5252771A (en) | Aluminum trifluoride catalyst for production of diaryl carbonates | |
| JP3755834B2 (ja) | アリールカーボネートの製造方法 | |
| KR100863662B1 (ko) | 방향족 카르보네이트의 제조 방법 | |
| JPH0123466B2 (enExample) | ||
| JPH1017529A (ja) | アリールカーボネートの連続製造法 | |
| US5980445A (en) | Process for producing diaryl carbonate | |
| BRPI0707429A2 (pt) | processos para a produção de carbonato de alquileno, e, para a preparação de alcano diol e carbonato de dialquila | |
| JP3546100B2 (ja) | ジアリールカーボネートの製造方法 | |
| JP3531298B2 (ja) | ジアリールカーボネート製造用触媒 | |
| US3234262A (en) | Process for preparing diaryl carbonates | |
| JP2889231B2 (ja) | 複素環系を含む芳香族化合物の製造方法 | |
| US5183919A (en) | Process for the preparation of diaryl carbonates | |
| US6160160A (en) | Process for preparing benzyl carbazates | |
| JP2804132B2 (ja) | カルバミン酸エステルの精製方法 | |
| JPH1077250A (ja) | 炭酸ジフェニルの製造法 | |
| US6175017B1 (en) | Process for the production of aryl carbonates | |
| JPH09278714A (ja) | 炭酸ジアリールの製造方法 |