GB1387319A - Process for the preparation of phosphonic acid dihalides - Google Patents
Process for the preparation of phosphonic acid dihalidesInfo
- Publication number
- GB1387319A GB1387319A GB4923772A GB4923772A GB1387319A GB 1387319 A GB1387319 A GB 1387319A GB 4923772 A GB4923772 A GB 4923772A GB 4923772 A GB4923772 A GB 4923772A GB 1387319 A GB1387319 A GB 1387319A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- phosphonic acid
- group
- hal
- halide
- 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
Links
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 title abstract 5
- -1 monothio Chemical class 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 3
- 150000004820 halides Chemical class 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical group ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 150000005690 diesters Chemical class 0.000 abstract 1
- XQRLCLUYWUNEEH-UHFFFAOYSA-N diphosphonic acid Chemical compound OP(=O)OP(O)=O XQRLCLUYWUNEEH-UHFFFAOYSA-N 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003007 phosphonic acid derivatives Chemical class 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/42—Halides thereof
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)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
1387319 Preparing phosphonic acid dihalides HOECHST AG 25 Oct 1972 [26 Oct 1971 26 Aug 1972] 49237/72 Heading C2P A phosphonic acid dihalide of the formula R-P(O)(Hal) 2 wherein R is an α,#-unsaturated alkenyl group having 2 to 18 carbon atoms, an α,#-unsaturated cycloalkenyl group having 3 to 10 carbon atoms, or a phenyl or benzyl group and wherein R may be substituted by a Cl or Br atom or by a C 1 -C 4 alkyl or -alkoxy group, cyano or CF 3 group and Hal is a halogen atom, is obtained by reacting a corresponding phosphonic or pyrophosphonic acid of the formulae RP(O)(OH) 2 and RP(O)(OH)OP(O)(OH)R, their monothio analogues or their functional derivatives with an acid halide (CO) n Hal 2 in which n is 1 or 2. The preferred acid halide is phosgene and the reaction is suitably effected at from 65‹ to 200‹ C. the acid halide being advantageously introduced into the phosphonic acid derivative optionally dissolved in an inert solvent which is preferably the end product of the reaction. A polymerization inhibitor may be included in the reaction mixture, especially when R is alkenyl. The phosphonic acid may be used in the form of a functional derivative, e.g. a semi-ester, diester, salt, ester halide, anhydride, pyrophosphonic acid ester or semiester or monothio analogue.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19712153149 DE2153149C3 (en) | 1971-10-26 | 1971-10-26 | Process for the preparation of phosphonic acid dihalides |
DE19722241993 DE2241993C3 (en) | 1972-08-26 | 1972-08-26 | Process for the preparation of phosphonic acid dihalides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1387319A true GB1387319A (en) | 1975-03-12 |
Family
ID=25761948
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4923772A Expired GB1387319A (en) | 1971-10-26 | 1972-10-25 | Process for the preparation of phosphonic acid dihalides |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPS4849724A (en) |
BE (1) | BE790584A (en) |
CA (1) | CA989416A (en) |
CH (1) | CH586231A5 (en) |
FR (1) | FR2158288B1 (en) |
GB (1) | GB1387319A (en) |
IT (1) | IT969854B (en) |
NL (1) | NL7214241A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3627009A1 (en) * | 1986-08-09 | 1988-02-18 | Hoechst Ag | METHOD FOR PRODUCING THIOPHOSPHINE ACID CHLORIDES |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3179696A (en) * | 1954-01-15 | 1965-04-20 | Olin Mathieson | Preparation of methane phosphonyl dichloride via phosgenation |
US3200145A (en) * | 1964-03-22 | 1965-08-10 | Olin Mathieson | Manufacture of methyl dichloro-phosphine oxide |
-
1972
- 1972-10-20 NL NL7214241A patent/NL7214241A/xx not_active Application Discontinuation
- 1972-10-23 CH CH1543772A patent/CH586231A5/xx not_active IP Right Cessation
- 1972-10-24 IT IT3087472A patent/IT969854B/en active
- 1972-10-24 JP JP10589872A patent/JPS4849724A/ja active Pending
- 1972-10-25 GB GB4923772A patent/GB1387319A/en not_active Expired
- 1972-10-25 CA CA154,781A patent/CA989416A/en not_active Expired
- 1972-10-26 FR FR7237997A patent/FR2158288B1/fr not_active Expired
- 1972-10-26 BE BE790584D patent/BE790584A/en unknown
Also Published As
Publication number | Publication date |
---|---|
FR2158288A1 (en) | 1973-06-15 |
IT969854B (en) | 1974-04-10 |
JPS4849724A (en) | 1973-07-13 |
NL7214241A (en) | 1973-05-01 |
CH586231A5 (en) | 1977-03-31 |
BE790584A (en) | 1973-04-26 |
CA989416A (en) | 1976-05-18 |
FR2158288B1 (en) | 1976-04-23 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |