DD233846A5 - Verfahren zur herstellung von triarylphosphaten - Google Patents
Verfahren zur herstellung von triarylphosphaten Download PDFInfo
- Publication number
- DD233846A5 DD233846A5 DD84269426A DD26942684A DD233846A5 DD 233846 A5 DD233846 A5 DD 233846A5 DD 84269426 A DD84269426 A DD 84269426A DD 26942684 A DD26942684 A DD 26942684A DD 233846 A5 DD233846 A5 DD 233846A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- phosphorylation
- reaction
- triaryl phosphates
- product
- phosphates
- Prior art date
Links
- 229910019142 PO4 Inorganic materials 0.000 title claims abstract description 36
- 238000000034 method Methods 0.000 title claims abstract description 34
- 230000008569 process Effects 0.000 title claims abstract description 21
- 238000002360 preparation method Methods 0.000 title claims abstract description 11
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title description 9
- 235000021317 phosphate Nutrition 0.000 claims abstract description 35
- 238000006366 phosphorylation reaction Methods 0.000 claims abstract description 28
- 230000026731 phosphorylation Effects 0.000 claims abstract description 24
- 239000003054 catalyst Substances 0.000 claims abstract description 18
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims abstract description 18
- -1 isopropylphenyl Chemical group 0.000 claims description 13
- 150000002989 phenols Chemical class 0.000 claims description 13
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 12
- 230000000865 phosphorylative effect Effects 0.000 claims description 12
- 239000007858 starting material Substances 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical class OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 3
- 230000002152 alkylating effect Effects 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 19
- 239000000047 product Substances 0.000 abstract description 14
- 238000000746 purification Methods 0.000 abstract description 11
- 239000007795 chemical reaction product Substances 0.000 abstract description 10
- 239000012264 purified product Substances 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 description 17
- 238000002474 experimental method Methods 0.000 description 16
- 238000005804 alkylation reaction Methods 0.000 description 10
- 238000004821 distillation Methods 0.000 description 10
- 230000029936 alkylation Effects 0.000 description 9
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 5
- CRBJBYGJVIBWIY-UHFFFAOYSA-N 2-isopropylphenol Chemical compound CC(C)C1=CC=CC=C1O CRBJBYGJVIBWIY-UHFFFAOYSA-N 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 150000003014 phosphoric acid esters Chemical class 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 1
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical group CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 1
- MEEKGULDSDXFCN-UHFFFAOYSA-N 2-pentylphenol Chemical group CCCCCC1=CC=CC=C1O MEEKGULDSDXFCN-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 239000001825 Polyoxyethene (8) stearate Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000004148 curcumin Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004245 inosinic acid Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- UXCDUFKZSUBXGM-UHFFFAOYSA-N phosphoric tribromide Chemical compound BrP(Br)(Br)=O UXCDUFKZSUBXGM-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/12—Esters of phosphoric acids with hydroxyaryl compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (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 |
|---|---|---|---|
| US06/551,641 US4559184A (en) | 1983-11-14 | 1983-11-14 | Phosphate ester synthesis without phosphorylation catalyst |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD233846A5 true DD233846A5 (de) | 1986-03-12 |
Family
ID=24202095
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD84269426A DD233846A5 (de) | 1983-11-14 | 1984-11-13 | Verfahren zur herstellung von triarylphosphaten |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4559184A (fr) |
| EP (1) | EP0142148B1 (fr) |
| JP (1) | JPS60105688A (fr) |
| CA (1) | CA1221981A (fr) |
| DD (1) | DD233846A5 (fr) |
| DE (1) | DE3479660D1 (fr) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0324716A3 (fr) * | 1988-01-12 | 1990-05-16 | Fmc Corporation (Uk) Limited | Phosphates triaryliques |
| DE10242710A1 (de) * | 2002-09-13 | 2004-04-08 | Daimlerchrysler Ag | Verfahren zum Herstellen eines Verbindungsbereiches auf einem Werkstück |
| EP2021347A2 (fr) * | 2006-04-24 | 2009-02-11 | Albermarle Corporation | Isopropylphénylphosphates à faible teneur en triphénylphosphate et à teneur élevée en phosphore d'alkylation ortho importante |
| KR102364281B1 (ko) * | 2020-12-04 | 2022-02-17 | 한서대학교 산학협력단 | 동일방향 액체분사가 가능한 다목적 드론 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1425392A (en) * | 1921-04-12 | 1922-08-08 | Corp Of Chem Fab Griesheim Ele | New liquid phosphoric esters and processes of making same |
| US1958210A (en) * | 1932-07-01 | 1934-05-08 | Kavalco Products Inc | Method of making aryl phosphates and product thereof |
| US2168587A (en) * | 1934-01-12 | 1939-08-08 | Celluloid Corp | Solvent and solution of cellulose esters |
| US2078421A (en) * | 1934-04-13 | 1937-04-27 | Celluloid Corp | Manufacture of alkyl and aryl phosphates |
| US3105846A (en) * | 1961-03-08 | 1963-10-01 | Celanese Corp | Process for producing aryl phosphate esters |
| US4139487A (en) * | 1965-12-01 | 1979-02-13 | Albright & Wilson Limited | Mixed tri-aryl (phenyl and alkylphenyl) phosphate esters |
| USRE29540E (en) * | 1966-06-18 | 1978-02-14 | Ciba-Geigy Ag | Phosphorylated alkylphenol/phenol ester mixtures |
| US4305789A (en) * | 1980-03-05 | 1981-12-15 | Prahl Walter H | Energy efficient process of preparing triaryl phosphates |
| US4351780A (en) * | 1980-12-09 | 1982-09-28 | Stauffer Chemical Company | Process for preparing isopropylphenyl/phenyl phosphate |
-
1983
- 1983-11-14 US US06/551,641 patent/US4559184A/en not_active Expired - Lifetime
-
1984
- 1984-09-17 CA CA000463342A patent/CA1221981A/fr not_active Expired
- 1984-10-16 JP JP59215289A patent/JPS60105688A/ja active Granted
- 1984-11-11 DE DE8484113612T patent/DE3479660D1/de not_active Expired
- 1984-11-11 EP EP84113612A patent/EP0142148B1/fr not_active Expired
- 1984-11-13 DD DD84269426A patent/DD233846A5/de unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60105688A (ja) | 1985-06-11 |
| JPH0460475B2 (fr) | 1992-09-28 |
| EP0142148B1 (fr) | 1989-09-06 |
| EP0142148A2 (fr) | 1985-05-22 |
| EP0142148A3 (en) | 1985-10-16 |
| DE3479660D1 (en) | 1989-10-12 |
| CA1221981A (fr) | 1987-05-19 |
| US4559184A (en) | 1985-12-17 |
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