PL407781A1 - 3,3,5,5-Tetra(dihydroxy phosphoryl)biphenyl and method of manufacturing it - Google Patents
3,3,5,5-Tetra(dihydroxy phosphoryl)biphenyl and method of manufacturing itInfo
- Publication number
- PL407781A1 PL407781A1 PL407781A PL40778114A PL407781A1 PL 407781 A1 PL407781 A1 PL 407781A1 PL 407781 A PL407781 A PL 407781A PL 40778114 A PL40778114 A PL 40778114A PL 407781 A1 PL407781 A1 PL 407781A1
- Authority
- PL
- Poland
- Prior art keywords
- biphenyl
- tetra
- tetrabromobiphenyl
- dihydroxyphosphoryl
- manufacturing
- Prior art date
Links
- NNPMHVXPDNEIPN-UHFFFAOYSA-N (3-phenyl-1,5,5-triphosphonocyclohex-2-en-1-yl)phosphonic acid Chemical group OP(=O)(O)C1(CC(=CC(C1)(P(=O)(O)O)P(=O)(O)O)C1=CC=CC=C1)P(=O)(O)O NNPMHVXPDNEIPN-UHFFFAOYSA-N 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- FXJXZYWFJAXIJX-UHFFFAOYSA-N 1,3-dibromo-5-(3,5-dibromophenyl)benzene Chemical group BrC1=CC(Br)=CC(C=2C=C(Br)C=C(Br)C=2)=C1 FXJXZYWFJAXIJX-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 abstract 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 abstract 2
- NDEHYSJCDSTVKK-UHFFFAOYSA-N CC(C)OP(C1=CC(C2=CC(P(OC(C)C)(OC(C)C)=O)=CC(P(OC(C)C)(OC(C)C)=O)=C2)=CC(P(OC(C)C)(OC(C)C)=O)=C1)(OC(C)C)=O Chemical group CC(C)OP(C1=CC(C2=CC(P(OC(C)C)(OC(C)C)=O)=CC(P(OC(C)C)(OC(C)C)=O)=C2)=CC(P(OC(C)C)(OC(C)C)=O)=C1)(OC(C)C)=O NDEHYSJCDSTVKK-UHFFFAOYSA-N 0.000 abstract 1
- MIYVPKNLWJFPGU-UHFFFAOYSA-N [3-(3,5-diphosphonophenyl)-5-phosphonophenyl]phosphonic acid Chemical group C1(=CC(=CC(=C1)P(O)(O)=O)P(O)(O)=O)C1=CC(=CC(=C1)P(O)(O)=O)P(O)(O)=O MIYVPKNLWJFPGU-UHFFFAOYSA-N 0.000 abstract 1
- 238000005903 acid hydrolysis reaction Methods 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- NFORZJQPTUSMRL-UHFFFAOYSA-N dipropan-2-yl hydrogen phosphite Chemical compound CC(C)OP(O)OC(C)C NFORZJQPTUSMRL-UHFFFAOYSA-N 0.000 abstract 1
- 229910052763 palladium Inorganic materials 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Wynalazek dotyczy 3,3',5,5'-tatra(dihydroksyfosforylo)bifelylu o wzorze 1 oraz sposób wytwarzania 3,3',5,5'-tatra(dihydroksyfosforylo)bifelylu o wzorze 1, który polega na tym, że do otrzymanego znaną metodą 3,3',5,5'-tetrabromobifenylu dodaje się fosforyn diizopropylowy w stosunku molowym 4,8:1 względem 3,3',5,5'-tetrabromobifenylu, diizopropyloetyloaminę w stosunku molowym 5,2:1 względem 3,3',5,5'-tetrabromobifenylu oraz katalizator palladowy i toluen jako rozpuszczalnik i otrzymuje się 3,3',5,5'-tetrakis(diizopropyloksyfosforylo)bifenyl, po czym w wyniku hydrolizy kwasowej za pomocą stężonego kwasu solnego otrzymuje się 3,3',5,5'-tetra(dihydroksyfosforylo)bifenyl.The invention relates to 3,3 ', 5,5'-tatra (dihydroxyphosphoryl) bifelyl of formula 1 and a process for producing 3,3', 5,5'-tatra (dihydroxyphosphoryl) bifelyl of formula 1, which consists in by the known 3,3 ', 5,5'-tetrabromobiphenyl method, diisopropyl phosphite is added in a molar ratio of 4.8: 1 relative to 3.3', 5.5'-tetrabromobiphenyl, diisopropylethylamine in a molar ratio of 5.2: 1 relative to 3, 3 ', 5,5'-tetrabromobiphenyl and a palladium catalyst and toluene as a solvent to obtain 3,3', 5,5'-tetrakis (diisopropyloxyphosphoryl) biphenyl, followed by acid hydrolysis with concentrated hydrochloric acid to give 3, 3 ', 5,5'-tetra (dihydroxyphosphoryl) biphenyl.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL407781A PL225597B1 (en) | 2014-04-03 | 2014-04-03 | 3,3,5,5-Tetra(dihydroxy phosphoryl)biphenyl and method of manufacturing it |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL407781A PL225597B1 (en) | 2014-04-03 | 2014-04-03 | 3,3,5,5-Tetra(dihydroxy phosphoryl)biphenyl and method of manufacturing it |
Publications (2)
Publication Number | Publication Date |
---|---|
PL407781A1 true PL407781A1 (en) | 2015-02-16 |
PL225597B1 PL225597B1 (en) | 2017-04-28 |
Family
ID=52464721
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL407781A PL225597B1 (en) | 2014-04-03 | 2014-04-03 | 3,3,5,5-Tetra(dihydroxy phosphoryl)biphenyl and method of manufacturing it |
Country Status (1)
Country | Link |
---|---|
PL (1) | PL225597B1 (en) |
-
2014
- 2014-04-03 PL PL407781A patent/PL225597B1/en unknown
Also Published As
Publication number | Publication date |
---|---|
PL225597B1 (en) | 2017-04-28 |
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