CA1330616C - Procede d'obtention de n(dichlorophosphoryl) trichlorophosphazene a partir de pentachlorure de phosphore et de chlorure d'ammonium - Google Patents
Procede d'obtention de n(dichlorophosphoryl) trichlorophosphazene a partir de pentachlorure de phosphore et de chlorure d'ammoniumInfo
- Publication number
- CA1330616C CA1330616C CA000551498A CA551498A CA1330616C CA 1330616 C CA1330616 C CA 1330616C CA 000551498 A CA000551498 A CA 000551498A CA 551498 A CA551498 A CA 551498A CA 1330616 C CA1330616 C CA 1330616C
- Authority
- CA
- Canada
- Prior art keywords
- temperature
- pcl5
- nh4cl
- trichlorophosphazene
- pocl3
- 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 - Fee Related
Links
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 238000000034 method Methods 0.000 title claims abstract description 21
- 235000019270 ammonium chloride Nutrition 0.000 title claims abstract description 14
- 238000002360 preparation method Methods 0.000 title abstract description 6
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 title description 6
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000012429 reaction media Substances 0.000 claims abstract description 12
- 229910019213 POCl3 Inorganic materials 0.000 claims abstract description 9
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical compound CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 claims abstract description 7
- -1 dichloro-phosphoryl Chemical group 0.000 claims abstract description 4
- FXTTXRHGRZVUAG-UHFFFAOYSA-N P.Cl.Cl.Cl.Cl.Cl Chemical compound P.Cl.Cl.Cl.Cl.Cl FXTTXRHGRZVUAG-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 3
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 230000004927 fusion Effects 0.000 claims 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 claims 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 28
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 238000004821 distillation Methods 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000000354 decomposition reaction Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- IUYHQGMDSZOPDZ-UHFFFAOYSA-N 2,3,4-trichlorobiphenyl Chemical group ClC1=C(Cl)C(Cl)=CC=C1C1=CC=CC=C1 IUYHQGMDSZOPDZ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 101100166829 Mus musculus Cenpk gene Proteins 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000003028 elevating effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000003385 sodium Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/02—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing phosphorus
- C08G79/025—Polyphosphazenes
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/082—Compounds containing nitrogen and non-metals and optionally metals
- C01B21/097—Compounds containing nitrogen and non-metals and optionally metals containing phosphorus atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Lubricants (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Luminescent Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8615684 | 1986-11-12 | ||
| FR8615684A FR2606396B1 (fr) | 1986-11-12 | 1986-11-12 | Procede d'obtention de n(dichlorophosphoryl) trichlorophosphazene a partir de pentachlorure de phosphore et de chlorure d'ammonium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1330616C true CA1330616C (fr) | 1994-07-12 |
Family
ID=9340717
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000551498A Expired - Fee Related CA1330616C (fr) | 1986-11-12 | 1987-11-10 | Procede d'obtention de n(dichlorophosphoryl) trichlorophosphazene a partir de pentachlorure de phosphore et de chlorure d'ammonium |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4780292A (enExample) |
| EP (1) | EP0269506B1 (enExample) |
| JP (1) | JPS63166706A (enExample) |
| KR (1) | KR940009270B1 (enExample) |
| CN (1) | CN1013660B (enExample) |
| AT (1) | ATE56684T1 (enExample) |
| CA (1) | CA1330616C (enExample) |
| DE (1) | DE3765093D1 (enExample) |
| DK (1) | DK169251B1 (enExample) |
| ES (1) | ES2017745B3 (enExample) |
| FI (1) | FI84166C (enExample) |
| FR (1) | FR2606396B1 (enExample) |
| GR (1) | GR3000951T3 (enExample) |
| IE (1) | IE60122B1 (enExample) |
| PT (1) | PT86112B (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5403909A (en) * | 1993-07-15 | 1995-04-04 | General Electric Company | Catalysts for polycondensation and redistribution of organosiloxane polymers |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA730618A (en) * | 1966-03-22 | Olin Mathieson Chemical Corporation | Preparation of p4n2ci14 | |
| CA724556A (en) * | 1965-12-28 | Lehr Wendel | Preparation of p3ncl12 | |
| CA572951A (en) * | 1959-03-24 | Barth-Wehrenalp Gerhard | Phosphorus compounds and process for making | |
| CA580958A (en) * | 1959-08-04 | J. Kahler Ernest | Compounds of the class p2x5no and process for producing same | |
| US2925320A (en) * | 1956-02-16 | 1960-02-16 | Pennsalt Chemicals Corp | Compounds of the class p2x5no and process for producing same |
| US3231327A (en) * | 1961-11-13 | 1966-01-25 | Fmc Corp | Preparation of n-dichlorophosphinylimidophosphoric trichloride |
| GB1321102A (en) * | 1970-04-09 | 1973-06-20 | Castrol Ltd | Method for preparing trihalophosphazine phosphoryl dihalides |
| FR2466435A1 (fr) * | 1979-09-27 | 1981-04-10 | Inst Mondial Phosphate | Nouveaux polychlorophosphazenes et leur procede de preparation |
| US4522798A (en) * | 1983-09-08 | 1985-06-11 | Ethyl Corporation | Halophosphazene polymers |
-
1986
- 1986-11-12 FR FR8615684A patent/FR2606396B1/fr not_active Expired
-
1987
- 1987-11-06 JP JP62280854A patent/JPS63166706A/ja active Granted
- 1987-11-09 DE DE8787402526T patent/DE3765093D1/de not_active Expired - Fee Related
- 1987-11-09 EP EP87402526A patent/EP0269506B1/fr not_active Expired - Lifetime
- 1987-11-09 ES ES87402526T patent/ES2017745B3/es not_active Expired - Lifetime
- 1987-11-09 AT AT87402526T patent/ATE56684T1/de active
- 1987-11-10 CA CA000551498A patent/CA1330616C/fr not_active Expired - Fee Related
- 1987-11-11 PT PT86112A patent/PT86112B/pt not_active IP Right Cessation
- 1987-11-11 DK DK591187A patent/DK169251B1/da not_active IP Right Cessation
- 1987-11-11 IE IE304287A patent/IE60122B1/en not_active IP Right Cessation
- 1987-11-11 FI FI874983A patent/FI84166C/fi not_active IP Right Cessation
- 1987-11-12 US US07/119,195 patent/US4780292A/en not_active Expired - Lifetime
- 1987-11-12 KR KR1019870012753A patent/KR940009270B1/ko not_active Expired - Fee Related
- 1987-11-12 CN CN87107375A patent/CN1013660B/zh not_active Expired
-
1990
- 1990-10-18 GR GR90400779T patent/GR3000951T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0481522B2 (enExample) | 1992-12-24 |
| GR3000951T3 (en) | 1991-12-10 |
| DK591187D0 (da) | 1987-11-11 |
| CN1013660B (zh) | 1991-08-28 |
| CN87107375A (zh) | 1988-06-22 |
| DK591187A (da) | 1988-05-13 |
| PT86112A (fr) | 1987-12-01 |
| FI84166B (fi) | 1991-07-15 |
| IE873042L (en) | 1988-05-12 |
| DK169251B1 (da) | 1994-09-26 |
| EP0269506A1 (fr) | 1988-06-01 |
| KR880006253A (ko) | 1988-07-22 |
| JPS63166706A (ja) | 1988-07-09 |
| EP0269506B1 (fr) | 1990-09-19 |
| US4780292A (en) | 1988-10-25 |
| FR2606396B1 (fr) | 1989-02-10 |
| FI874983L (fi) | 1988-05-13 |
| ATE56684T1 (de) | 1990-10-15 |
| IE60122B1 (en) | 1994-06-01 |
| FR2606396A1 (fr) | 1988-05-13 |
| DE3765093D1 (de) | 1990-10-25 |
| PT86112B (pt) | 1990-08-31 |
| ES2017745B3 (es) | 1991-03-01 |
| FI84166C (fi) | 1991-10-25 |
| FI874983A0 (fi) | 1987-11-11 |
| KR940009270B1 (ko) | 1994-10-06 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKLA | Lapsed |