SU1739843A3 - Способ получени окси-и метоксипроизводных дифенилметана - Google Patents
Способ получени окси-и метоксипроизводных дифенилметана Download PDFInfo
- Publication number
- SU1739843A3 SU1739843A3 SU874203612A SU4203612A SU1739843A3 SU 1739843 A3 SU1739843 A3 SU 1739843A3 SU 874203612 A SU874203612 A SU 874203612A SU 4203612 A SU4203612 A SU 4203612A SU 1739843 A3 SU1739843 A3 SU 1739843A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- zeolite
- phenol
- reaction
- zeolites
- derivatives
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 11
- 238000002360 preparation method Methods 0.000 title abstract description 7
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 title abstract description 6
- 239000010457 zeolite Substances 0.000 claims abstract description 46
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 35
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 35
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 29
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910001868 water Inorganic materials 0.000 claims abstract description 20
- 238000006243 chemical reaction Methods 0.000 claims abstract description 18
- 229910052681 coesite Inorganic materials 0.000 claims abstract description 18
- 229910052906 cristobalite Inorganic materials 0.000 claims abstract description 18
- 229910052682 stishovite Inorganic materials 0.000 claims abstract description 18
- 229910052905 tridymite Inorganic materials 0.000 claims abstract description 18
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 17
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 claims abstract description 16
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000003054 catalyst Substances 0.000 claims abstract description 12
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 claims abstract description 8
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims abstract description 8
- 238000009833 condensation Methods 0.000 claims abstract description 7
- 230000005494 condensation Effects 0.000 claims abstract description 7
- 239000004005 microsphere Substances 0.000 claims abstract description 6
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 6
- 239000002904 solvent Substances 0.000 claims abstract description 5
- 238000009835 boiling Methods 0.000 claims abstract description 4
- 238000002441 X-ray diffraction Methods 0.000 claims abstract description 3
- 239000012442 inert solvent Substances 0.000 claims abstract description 3
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 3
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims abstract 3
- 238000002329 infrared spectrum Methods 0.000 claims description 6
- 239000003153 chemical reaction reagent Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000000376 reactant Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 17
- 238000001228 spectrum Methods 0.000 abstract description 3
- -1 nitrogenous organic base Chemical class 0.000 description 28
- 239000000243 solution Substances 0.000 description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 239000000047 product Substances 0.000 description 13
- 238000003756 stirring Methods 0.000 description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 10
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 9
- 239000000725 suspension Substances 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 150000004679 hydroxides Chemical class 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- JMXKSZRRTHPKDL-UHFFFAOYSA-N titanium ethoxide Chemical compound [Ti+4].CC[O-].CC[O-].CC[O-].CC[O-] JMXKSZRRTHPKDL-UHFFFAOYSA-N 0.000 description 6
- 239000003513 alkali Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 150000003376 silicon Chemical class 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 238000004949 mass spectrometry Methods 0.000 description 4
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 4
- 150000003608 titanium Chemical class 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000008267 milk Substances 0.000 description 3
- 210000004080 milk Anatomy 0.000 description 3
- 235000013336 milk Nutrition 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 239000013049 sediment Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 150000001638 boron Chemical class 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000008098 formaldehyde solution Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000012456 homogeneous solution Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LPSKDVINWQNWFE-UHFFFAOYSA-M tetrapropylazanium;hydroxide Chemical compound [OH-].CCC[N+](CCC)(CCC)CCC LPSKDVINWQNWFE-UHFFFAOYSA-M 0.000 description 2
- HEVMDQBCAHEHDY-UHFFFAOYSA-N (Dimethoxymethyl)benzene Chemical compound COC(OC)C1=CC=CC=C1 HEVMDQBCAHEHDY-UHFFFAOYSA-N 0.000 description 1
- UGACIEPFGXRWCH-UHFFFAOYSA-N [Si].[Ti] Chemical class [Si].[Ti] UGACIEPFGXRWCH-UHFFFAOYSA-N 0.000 description 1
- NYRVXYOKUZSUDA-UHFFFAOYSA-N [dimethoxy(phenyl)methyl]benzene Chemical compound C=1C=CC=CC=1C(OC)(OC)C1=CC=CC=C1 NYRVXYOKUZSUDA-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- KQQCTWHSWXCZHB-UHFFFAOYSA-N azane;propan-2-ol Chemical compound N.CC(C)O KQQCTWHSWXCZHB-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-O azanium;hydron;hydroxide Chemical compound [NH4+].O VHUUQVKOLVNVRT-UHFFFAOYSA-O 0.000 description 1
- GHXRKGHKMRZBJH-UHFFFAOYSA-N boric acid Chemical compound OB(O)O.OB(O)O GHXRKGHKMRZBJH-UHFFFAOYSA-N 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 150000002505 iron Chemical class 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 238000003760 magnetic stirring Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052680 mordenite Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- JAJLKEVKNDUJBG-UHFFFAOYSA-N perfluorotripropylamine Chemical compound FC(F)(F)C(F)(F)C(F)(F)N(C(F)(F)C(F)(F)C(F)(F)F)C(F)(F)C(F)(F)C(F)(F)F JAJLKEVKNDUJBG-UHFFFAOYSA-N 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- AJSTXXYNEIHPMD-UHFFFAOYSA-N triethyl borate Chemical compound CCOB(OCC)OCC AJSTXXYNEIHPMD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/12—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings
- C07C39/15—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring polycyclic with no unsaturation outside the aromatic rings with all hydroxy groups on non-condensed rings, e.g. phenylphenol
- C07C39/16—Bis-(hydroxyphenyl) alkanes; Tris-(hydroxyphenyl)alkanes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
- C07C41/30—Preparation of ethers by reactions not forming ether-oxygen bonds by increasing the number of carbon atoms, e.g. by oligomerisation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/86—Borosilicates; Aluminoborosilicates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/89—Silicates, aluminosilicates or borosilicates of titanium, zirconium or hafnium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
- C07C37/115—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms using acetals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
- C07C37/20—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms using aldehydes or ketones
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polyesters Or Polycarbonates (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT8622073A IT1213366B (it) | 1986-10-22 | 1986-10-22 | Procedimento per la condensazione tra composti aromatici e carbonilici. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1739843A3 true SU1739843A3 (ru) | 1992-06-07 |
Family
ID=11191071
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU874203612A SU1739843A3 (ru) | 1986-10-22 | 1987-10-21 | Способ получени окси-и метоксипроизводных дифенилметана |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4895988A (enExample) |
| EP (1) | EP0265017B1 (enExample) |
| JP (1) | JPS63115830A (enExample) |
| KR (1) | KR910000248B1 (enExample) |
| AT (1) | ATE74343T1 (enExample) |
| BR (1) | BR8705831A (enExample) |
| CA (1) | CA1315298C (enExample) |
| DE (1) | DE3777943D1 (enExample) |
| DK (1) | DK547987A (enExample) |
| ES (1) | ES2031879T3 (enExample) |
| GR (1) | GR3004737T3 (enExample) |
| IT (1) | IT1213366B (enExample) |
| MX (1) | MX168852B (enExample) |
| SU (1) | SU1739843A3 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03139519A (ja) * | 1989-10-25 | 1991-06-13 | Sumitomo Chem Co Ltd | エポキシ樹脂用硬化剤 |
| US5877362A (en) * | 1996-09-12 | 1999-03-02 | Nippon Petrochemicals Company, Limited | Method for producing diphenylmethane |
| US5880322A (en) * | 1996-12-16 | 1999-03-09 | Nippen Petrochemicals Company, Limited | Method for producing diarylmethane |
| US5856575A (en) * | 1997-01-22 | 1999-01-05 | Council Of Scientific Industrial Research | Process for the preparation of N-acetyl aminophenols |
| US6207866B1 (en) * | 1997-07-11 | 2001-03-27 | Nippon Petrochemicals Company, Limited | Method for producing diarylmethane or its derivatives |
| JP2000016952A (ja) | 1998-07-01 | 2000-01-18 | Nippon Petrochem Co Ltd | 炭化水素の製造方法 |
| WO2000039059A1 (en) * | 1998-12-30 | 2000-07-06 | Mobil Oil Corporation | Synthesis of bisphenols |
| US6492566B1 (en) * | 1999-02-25 | 2002-12-10 | Council Of Scientific And Industrial Research | Process for the preparation of dihydroxydiphenylmethanes |
| JP4376367B2 (ja) | 1999-09-20 | 2009-12-02 | 新日本石油株式会社 | 炭化水素溶剤およびそれを用いた感圧複写材料 |
| ITMI20011143A1 (it) * | 2001-05-30 | 2002-11-30 | Enitecnologie Spa | Processo per la preparazionee di bisfenoli con zeoliti |
| JP2003002848A (ja) * | 2001-06-20 | 2003-01-08 | Nippon Petrochemicals Co Ltd | ジアリールメタンおよびその誘導体の製造方法 |
| CN1326815C (zh) * | 2005-01-14 | 2007-07-18 | 浙江大学 | 二甲基二苯甲烷的催化合成工艺 |
| DE102010062804A1 (de) * | 2010-01-12 | 2011-07-14 | Evonik Degussa GmbH, 45128 | Verfahren zur Herstellung von 1,1 Diarylalkanen und Derivativen davon |
| CN116082124B (zh) * | 2022-11-14 | 2024-06-18 | 江苏扬农锦湖化工有限公司 | 一种4,4-二羟基二苯基甲烷的制备方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4243828A (en) * | 1963-02-27 | 1981-01-06 | Mobil Oil Corporation | Alkylation of aromatics using a high silica zeolite |
| US3496239A (en) * | 1965-03-05 | 1970-02-17 | Mobil Oil Corp | Production of aromatic condensation products |
| US3728408A (en) * | 1969-05-05 | 1973-04-17 | Mobil Oil Corp | Conversion of polar compounds using highly siliceous zeolite-type catalysts |
| US4317944A (en) * | 1980-08-15 | 1982-03-02 | General Electric Company | Preparation of 2,2-bis(4-hydroxyphenyl) propane |
| FI76005C (fi) * | 1983-10-17 | 1988-09-09 | Neste Oy | Aluminium-bor-silikatkatalysator, foerfarande foer framstaellning av denna och alkyleringsprocess. |
| IT1207520B (it) * | 1985-12-19 | 1989-05-25 | Eniricerche S P A Snamprogetti | Materiale sintetico cristallino poroso contenente ossidi di silicio titanio e ferro. |
| IT1207519B (it) * | 1985-12-19 | 1989-05-25 | Eniricerche Spa | Materiale sintetico cristallino poroso contenetne ossidi di silicio titanio e alluminio. |
| US4694111A (en) * | 1986-07-09 | 1987-09-15 | Celanese Corporation | Alkoxyalkylation of phenol |
-
1986
- 1986-10-22 IT IT8622073A patent/IT1213366B/it active
-
1987
- 1987-10-19 AT AT87202002T patent/ATE74343T1/de not_active IP Right Cessation
- 1987-10-19 ES ES198787202002T patent/ES2031879T3/es not_active Expired - Lifetime
- 1987-10-19 DE DE8787202002T patent/DE3777943D1/de not_active Expired - Lifetime
- 1987-10-19 EP EP87202002A patent/EP0265017B1/en not_active Expired - Lifetime
- 1987-10-20 US US07/110,329 patent/US4895988A/en not_active Expired - Fee Related
- 1987-10-20 DK DK547987A patent/DK547987A/da not_active Application Discontinuation
- 1987-10-21 CA CA000549872A patent/CA1315298C/en not_active Expired - Fee Related
- 1987-10-21 SU SU874203612A patent/SU1739843A3/ru active
- 1987-10-22 MX MX008951A patent/MX168852B/es unknown
- 1987-10-22 JP JP62265509A patent/JPS63115830A/ja active Pending
- 1987-10-22 BR BR8705831A patent/BR8705831A/pt not_active Application Discontinuation
- 1987-10-22 KR KR1019870011854A patent/KR910000248B1/ko not_active Expired
-
1992
- 1992-05-27 GR GR920401086T patent/GR3004737T3/el unknown
Non-Patent Citations (1)
| Title |
|---|
| Venuta P.В., Landis P.S. Organic reactions catalysed by crystalline alumos. licates III Condensation reactions by carbonyl compounds. J. Catalysis, 1966, v. 6, p. 237. Патент US № 3496239, кл. В 01. J 29/28, опублик. 1969. * |
Also Published As
| Publication number | Publication date |
|---|---|
| GR3004737T3 (enExample) | 1993-04-28 |
| DK547987D0 (da) | 1987-10-20 |
| CA1315298C (en) | 1993-03-30 |
| KR880005059A (ko) | 1988-06-27 |
| ES2031879T3 (es) | 1993-01-01 |
| JPS63115830A (ja) | 1988-05-20 |
| DE3777943D1 (de) | 1992-05-07 |
| EP0265017A2 (en) | 1988-04-27 |
| EP0265017B1 (en) | 1992-04-01 |
| DK547987A (da) | 1988-04-23 |
| IT8622073A0 (it) | 1986-10-22 |
| IT1213366B (it) | 1989-12-20 |
| MX168852B (es) | 1993-06-11 |
| BR8705831A (pt) | 1988-05-31 |
| EP0265017A3 (en) | 1989-02-22 |
| US4895988A (en) | 1990-01-23 |
| KR910000248B1 (ko) | 1991-01-23 |
| ATE74343T1 (de) | 1992-04-15 |
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