SU535910A3 - Способ получени трис-(2-хлорэтил) фосфита - Google Patents
Способ получени трис-(2-хлорэтил) фосфитаInfo
- Publication number
- SU535910A3 SU535910A3 SU1955016A SU1955016A SU535910A3 SU 535910 A3 SU535910 A3 SU 535910A3 SU 1955016 A SU1955016 A SU 1955016A SU 1955016 A SU1955016 A SU 1955016A SU 535910 A3 SU535910 A3 SU 535910A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- carried out
- solution
- phosphite
- reaction
- phosphonate
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 15
- LUVCTYHBTXSAMX-UHFFFAOYSA-N tris(2-chloroethyl) phosphite Chemical compound ClCCOP(OCCCl)OCCCl LUVCTYHBTXSAMX-UHFFFAOYSA-N 0.000 title claims description 6
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 claims description 11
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 10
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 9
- -1 tertiary amine halide Chemical class 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 19
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 16
- 238000002474 experimental method Methods 0.000 description 15
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 14
- 239000007795 chemical reaction product Substances 0.000 description 8
- 238000005481 NMR spectroscopy Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 6
- 238000007792 addition Methods 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- VNDYJBBGRKZCSX-UHFFFAOYSA-L zinc bromide Chemical compound Br[Zn]Br VNDYJBBGRKZCSX-UHFFFAOYSA-L 0.000 description 2
- NNPZIMOTVKYAGP-UHFFFAOYSA-N 4-chloro-2-hydroxy-1,3,2-dioxaphospholane Chemical compound OP1OCC(Cl)O1 NNPZIMOTVKYAGP-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- XHFGWHUWQXTGAT-UHFFFAOYSA-N dimethylamine hydrochloride Natural products CNC(C)C XHFGWHUWQXTGAT-UHFFFAOYSA-N 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000003840 hydrochlorides Chemical group 0.000 description 1
- BGMIRDHBNWQSGE-UHFFFAOYSA-N hypochlorous acid;pyridine Chemical compound ClO.C1=CC=NC=C1 BGMIRDHBNWQSGE-UHFFFAOYSA-N 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 229940102001 zinc bromide Drugs 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
- C07F9/141—Esters of phosphorous acids
- C07F9/1411—Esters of phosphorous acids with hydroxyalkyl compounds with further substituents on alkyl
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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Polyurethanes Or Polyureas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00283974A US3810961A (en) | 1972-08-25 | 1972-08-25 | Process for preparing tris(2-haloalkyl)phosphites |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU535910A3 true SU535910A3 (ru) | 1976-11-15 |
Family
ID=23088368
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1955016A SU535910A3 (ru) | 1972-08-25 | 1973-08-21 | Способ получени трис-(2-хлорэтил) фосфита |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3810961A (enExample) |
| JP (1) | JPS5120494B2 (enExample) |
| BE (1) | BE804013A (enExample) |
| CA (1) | CA989861A (enExample) |
| DE (1) | DE2338006B2 (enExample) |
| ES (1) | ES418152A1 (enExample) |
| FR (1) | FR2197010B1 (enExample) |
| GB (1) | GB1394356A (enExample) |
| IT (1) | IT989916B (enExample) |
| NL (1) | NL167966C (enExample) |
| SU (1) | SU535910A3 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3886239A (en) * | 1972-08-25 | 1975-05-27 | Olin Corp | Process for preparing tris (2-haloalkyl) phosphites |
| FR2218343B1 (enExample) * | 1973-02-21 | 1977-04-29 | Ugine Kuhlmann | |
| US3987129A (en) * | 1975-02-26 | 1976-10-19 | Olin Corporation | Process for preparing bis(2-haloalkyl) phosphoro-halidates |
| JPS527924A (en) * | 1975-07-09 | 1977-01-21 | Yotsukaichi Gosei Kk | Process for preparation of phosphorous ester containing halogen |
| US4218405A (en) * | 1978-04-26 | 1980-08-19 | Olin Corporation | Halogenated tertiary phosphite esters |
| US4308193A (en) * | 1978-04-26 | 1981-12-29 | Olin Corporation | Halogenated tertiary phosphite esters |
| US5041596A (en) * | 1989-07-03 | 1991-08-20 | Akzo America Inc. | Formation of glycol bisphosphate compounds |
-
1972
- 1972-08-25 US US00283974A patent/US3810961A/en not_active Expired - Lifetime
-
1973
- 1973-06-14 CA CA174,103A patent/CA989861A/en not_active Expired
- 1973-07-17 IT IT51521/73A patent/IT989916B/it active
- 1973-07-26 DE DE2338006A patent/DE2338006B2/de not_active Withdrawn
- 1973-07-31 FR FR7327977A patent/FR2197010B1/fr not_active Expired
- 1973-08-15 NL NL7311232A patent/NL167966C/xx not_active IP Right Cessation
- 1973-08-21 SU SU1955016A patent/SU535910A3/ru active
- 1973-08-23 GB GB4003373A patent/GB1394356A/en not_active Expired
- 1973-08-23 JP JP48093956A patent/JPS5120494B2/ja not_active Expired
- 1973-08-24 ES ES418152A patent/ES418152A1/es not_active Expired
- 1973-08-24 BE BE134926A patent/BE804013A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL7311232A (enExample) | 1974-02-27 |
| BE804013A (fr) | 1974-02-25 |
| IT989916B (it) | 1975-06-10 |
| CA989861A (en) | 1976-05-25 |
| US3810961A (en) | 1974-05-14 |
| FR2197010A1 (enExample) | 1974-03-22 |
| FR2197010B1 (enExample) | 1977-02-25 |
| ES418152A1 (es) | 1976-03-16 |
| NL167966B (nl) | 1981-09-16 |
| GB1394356A (en) | 1975-05-14 |
| JPS5120494B2 (enExample) | 1976-06-25 |
| NL167966C (nl) | 1982-02-16 |
| JPS4962423A (enExample) | 1974-06-17 |
| DE2338006B2 (de) | 1980-09-25 |
| DE2338006A1 (de) | 1974-03-07 |
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