CH666677A5 - Procede de valorisation sous forme de produits perbromes de produits sous-bromes obtenus en solutions. - Google Patents
Procede de valorisation sous forme de produits perbromes de produits sous-bromes obtenus en solutions. Download PDFInfo
- Publication number
- CH666677A5 CH666677A5 CH2694/86A CH269486A CH666677A5 CH 666677 A5 CH666677 A5 CH 666677A5 CH 2694/86 A CH2694/86 A CH 2694/86A CH 269486 A CH269486 A CH 269486A CH 666677 A5 CH666677 A5 CH 666677A5
- Authority
- CH
- Switzerland
- Prior art keywords
- products
- sub
- brominated
- subbrominated
- treated
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 31
- 239000000047 product Substances 0.000 claims description 34
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 16
- 239000003054 catalyst Substances 0.000 claims description 15
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 11
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 10
- 229910052794 bromium Inorganic materials 0.000 claims description 10
- 238000005893 bromination reaction Methods 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 230000031709 bromination Effects 0.000 claims description 8
- FJBFPHVGVWTDIP-UHFFFAOYSA-N dibromomethane Chemical group BrCBr FJBFPHVGVWTDIP-UHFFFAOYSA-N 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 8
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 7
- 125000001246 bromo group Chemical group Br* 0.000 claims description 6
- 230000008030 elimination Effects 0.000 claims description 5
- 238000003379 elimination reaction Methods 0.000 claims description 5
- 239000008346 aqueous phase Substances 0.000 claims description 4
- 239000012074 organic phase Substances 0.000 claims description 4
- 239000012429 reaction media Substances 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- -1 aluminum halide Chemical class 0.000 claims description 3
- 239000012071 phase Substances 0.000 claims description 3
- 238000011403 purification operation Methods 0.000 claims description 3
- 238000010992 reflux Methods 0.000 claims description 3
- 238000000926 separation method Methods 0.000 claims description 3
- 239000006228 supernatant Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 150000008282 halocarbons Chemical group 0.000 claims description 2
- 230000001131 transforming effect Effects 0.000 claims description 2
- 238000010908 decantation Methods 0.000 claims 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 22
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 125000006267 biphenyl group Chemical group 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- PUGUQINMNYINPK-UHFFFAOYSA-N tert-butyl 4-(2-chloroacetyl)piperazine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCN(C(=O)CCl)CC1 PUGUQINMNYINPK-UHFFFAOYSA-N 0.000 description 2
- ORYGKUIDIMIRNN-UHFFFAOYSA-N 1,2,3,4-tetrabromo-5-(2,3,4,5-tetrabromophenoxy)benzene Chemical compound BrC1=C(Br)C(Br)=CC(OC=2C(=C(Br)C(Br)=C(Br)C=2)Br)=C1Br ORYGKUIDIMIRNN-UHFFFAOYSA-N 0.000 description 1
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 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
- 239000003863 metallic catalyst Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- 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
- C07C41/22—Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of halogens; by substitution of halogen atoms by other halogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (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 |
|---|---|---|---|
| FR8510162A FR2584394B1 (fr) | 1985-07-03 | 1985-07-03 | Procede de valorisation sous-forme de produits perbromes de produits sous-bromes obtenus en solutions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH666677A5 true CH666677A5 (fr) | 1988-08-15 |
Family
ID=9320928
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH2694/86A CH666677A5 (fr) | 1985-07-03 | 1986-07-03 | Procede de valorisation sous forme de produits perbromes de produits sous-bromes obtenus en solutions. |
Country Status (10)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL80390A (en) * | 1986-10-22 | 1992-06-21 | Bromine Compounds Ltd | Process for the preparation of decabromodiphenyl ether |
| IL80391A (en) * | 1986-10-22 | 1992-03-29 | Bromine Compounds Ltd | Process for the preparation of decabromodiphenyl ether with improved thermal stability |
| WO2008027779A1 (en) * | 2006-08-29 | 2008-03-06 | Albemarle Corporation | Preparation of decabromodiphenyl oxide |
| WO2008027778A1 (en) * | 2006-08-29 | 2008-03-06 | Albemarle Corporation | Preparation of high assay decabromodiphenyl oxide |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3763248A (en) * | 1971-03-02 | 1973-10-02 | Ethyl Corp | Process for production of poly brominated aromatics |
| US3833674A (en) * | 1972-08-24 | 1974-09-03 | Ethyl Corp | Recovery of brominated biphenyl |
| JPS5239638A (en) * | 1975-08-25 | 1977-03-28 | Toyo Soda Mfg Co Ltd | Process for preparation of decabromobiphenylether |
| GB1472383A (en) * | 1976-01-23 | 1977-05-04 | Isc Chem Ltd | Bromination of diphenyl oxide |
| DD128749A1 (de) * | 1976-12-13 | 1977-12-07 | Wolfgang Baumann | Verfahren zur herstellung von hexabrombenzol |
| DD137803A3 (de) * | 1976-12-13 | 1979-09-26 | Hans Baltz | Verfahren zur herstellung von hexabrombenzol |
| US4521633A (en) * | 1983-05-19 | 1985-06-04 | The Dow Chemical Company | Bromination process |
-
1985
- 1985-07-03 FR FR8510162A patent/FR2584394B1/fr not_active Expired
-
1986
- 1986-06-24 NL NL8601648A patent/NL8601648A/nl not_active Application Discontinuation
- 1986-06-27 IT IT20961/86A patent/IT1190141B/it active
- 1986-06-30 IL IL79285A patent/IL79285A0/xx unknown
- 1986-07-02 GB GB8616122A patent/GB2177399B/en not_active Expired
- 1986-07-02 DE DE19863622235 patent/DE3622235A1/de active Granted
- 1986-07-02 BE BE0/216867A patent/BE905039A/fr not_active IP Right Cessation
- 1986-07-03 JP JP61157144A patent/JPS6210035A/ja active Pending
- 1986-07-03 ES ES8600100A patent/ES2000304A6/es not_active Expired
- 1986-07-03 CH CH2694/86A patent/CH666677A5/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| BE905039A (fr) | 1987-01-02 |
| NL8601648A (nl) | 1987-02-02 |
| IT8620961A0 (it) | 1986-06-27 |
| IL79285A0 (en) | 1986-09-30 |
| GB2177399B (en) | 1989-07-19 |
| FR2584394B1 (fr) | 1987-09-25 |
| GB2177399A (en) | 1987-01-21 |
| FR2584394A1 (fr) | 1987-01-09 |
| ES2000304A6 (es) | 1988-02-16 |
| JPS6210035A (ja) | 1987-01-19 |
| GB8616122D0 (en) | 1986-08-06 |
| IT8620961A1 (it) | 1987-12-27 |
| DE3622235C2 (enrdf_load_stackoverflow) | 1989-10-19 |
| IT1190141B (it) | 1988-02-10 |
| DE3622235A1 (de) | 1987-01-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased | ||
| PL | Patent ceased |