KR960041189A - Process for preparing phosphonate compound - Google Patents
Process for preparing phosphonate compound Download PDFInfo
- Publication number
- KR960041189A KR960041189A KR1019950012762A KR19950012762A KR960041189A KR 960041189 A KR960041189 A KR 960041189A KR 1019950012762 A KR1019950012762 A KR 1019950012762A KR 19950012762 A KR19950012762 A KR 19950012762A KR 960041189 A KR960041189 A KR 960041189A
- Authority
- KR
- South Korea
- Prior art keywords
- phosphite
- phosphonate compound
- alkyl group
- compound
- general formula
- Prior art date
Links
- -1 phosphonate compound Chemical class 0.000 title claims abstract 10
- 238000004519 manufacturing process Methods 0.000 title claims 5
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims abstract 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract 4
- 239000003054 catalyst Substances 0.000 claims abstract 4
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims abstract 2
- AHXGRMIPHCAXFP-UHFFFAOYSA-L chromyl dichloride Chemical compound Cl[Cr](Cl)(=O)=O AHXGRMIPHCAXFP-UHFFFAOYSA-L 0.000 claims abstract 2
- 229910052736 halogen Inorganic materials 0.000 claims abstract 2
- 150000002367 halogens Chemical class 0.000 claims abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 239000007983 Tris buffer Substances 0.000 claims 1
- 230000008707 rearrangement Effects 0.000 claims 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 claims 1
- CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 claims 1
- SJHCUXCOGGKFAI-UHFFFAOYSA-N tripropan-2-yl phosphite Chemical compound CC(C)OP(OC(C)C)OC(C)C SJHCUXCOGGKFAI-UHFFFAOYSA-N 0.000 claims 1
- RZIHJXIUVJCZNI-UHFFFAOYSA-N tris(2-bromopropyl) phosphite Chemical compound CC(Br)COP(OCC(C)Br)OCC(C)Br RZIHJXIUVJCZNI-UHFFFAOYSA-N 0.000 claims 1
- LUVCTYHBTXSAMX-UHFFFAOYSA-N tris(2-chloroethyl) phosphite Chemical compound ClCCOP(OCCCl)OCCCl LUVCTYHBTXSAMX-UHFFFAOYSA-N 0.000 claims 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)]
- C07F9/40—Esters 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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
본 발명은 다음의 일반식(Ⅰ)로 표시되는 포스포네이트 화합물을 크로밀클로라이드 함유 r형 알루미나 촉매 존재하에서 저온에서의 재배열을 통해서 일반식(Ⅱ)로 표시되는 포스포네이트 유도체를 제조하는 방법에 관한 것이다.The present invention provides a phosphonate derivative represented by the general formula (II) by rearranging the phosphonate compound represented by the following general formula (I) at a low temperature in the presence of a chromyl chloride-containing r-type alumina catalyst. It is about a method.
상기 일반식(Ⅰ) 및 (Ⅱ)에서 R은 C1∼C10의 알킬기 또는 할로겐원소가 치환된 C1∼C10의 알킬기를 나타낸다.In the general formulas (I) and (II), R represents a C 1 to C 10 alkyl group or a C 1 to C 10 alkyl group substituted with a halogen element.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019950012762A KR100341301B1 (en) | 1995-05-22 | 1995-05-22 | Process for production of phosphonate compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019950012762A KR100341301B1 (en) | 1995-05-22 | 1995-05-22 | Process for production of phosphonate compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
KR960041189A true KR960041189A (en) | 1996-12-19 |
KR100341301B1 KR100341301B1 (en) | 2002-10-25 |
Family
ID=37488204
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019950012762A KR100341301B1 (en) | 1995-05-22 | 1995-05-22 | Process for production of phosphonate compounds |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR100341301B1 (en) |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58194953A (en) * | 1982-05-08 | 1983-11-14 | Dai Ichi Kogyo Seiyaku Co Ltd | Flame retarder for synthetic resin |
US5142084A (en) * | 1991-10-11 | 1992-08-25 | Carter Charles G | Preparation of allylphosphonic acid |
JP3452374B2 (en) * | 1993-01-26 | 2003-09-29 | 三菱化学株式会社 | Method for producing benzylphosphonate derivative |
US5473093A (en) * | 1995-01-10 | 1995-12-05 | Akzo Nobel N.V. | Process for the synthesis of diethyl ethylphosphonate |
-
1995
- 1995-05-22 KR KR1019950012762A patent/KR100341301B1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
KR100341301B1 (en) | 2002-10-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ATE1242T1 (en) | PROCESS FOR THE PREPARATION OF 3-AMINO-1-HYDROXYPROPAN-1,1-DIPHOSPHONIC ACID. | |
NO862170L (en) | PREPARATION OF QUINAZOLINE DERIVATIVES. | |
DE69814635D1 (en) | METHOD FOR PRODUCING 2-HYDROXYBENZAMIDE DERIVATIVES | |
KR840004082A (en) | Pyridazide derivatives, preparation methods thereof, and agricultural and horticultural bactericidal, insecticidal and aphid insecticidal compositions containing the derivatives | |
KR960041189A (en) | Process for preparing phosphonate compound | |
ATE299870T1 (en) | METHOD FOR PRODUCING 1,4,7,10-TETRAAZADODECAN-1,4-DIACETIC ACID DERIVATIVES | |
ATE258905T1 (en) | METHOD FOR PRODUCING ALKANES | |
AR247736A1 (en) | A procedure for the preparation of piperazine derivatives | |
KR850001724A (en) | Method for preparing 4-phenyl-4-oxo-butene-2-pentophosphate derivative | |
KR890017264A (en) | Method for preparing N-phosphonomethyl glycine | |
BR9501451A (en) | Process composition for the stabilization of an organic phosphite or phosphonite and organic phosphite or phosphonite obtained | |
KR920017997A (en) | Method of Making Aldehyde | |
KR920009833A (en) | Method for preparing 3-alkoxymethyl sephalosporin derivative | |
KR850004587A (en) | Method for preparing substituted N-phenyl-N'-acylisothiourea | |
KR850002979A (en) | New Preparation Method of 1,2,3-Trithian Compound | |
ES491893A0 (en) | PROCEDURE FOR OBTAINING STABILIZED HALOGENATED HYDROCARBONS | |
DE69839732D1 (en) | PROCESS FOR THE PREPARATION OF 3,4-DIHYDROXY-3CYCLOBUTENE-1,2-DION | |
KR910011729A (en) | Method for preparing 2-hydroxybenzophenone derivative | |
KR930017893A (en) | Method for preparing a reactive dye having a sulfoalkyl-hydroxy pyridone group | |
KR900006295A (en) | Halogeno-4-methylpyrazoles and preparation method thereof | |
KR910011876A (en) | Complexes of rhodium containing sulfonated triphenylphosphane compounds | |
KR910019969A (en) | Prostaglandin I isotropes | |
ES2193548T3 (en) | PROCEDURE FOR THE PREPARATION OF DERIVATIVES 1,3-DIAZA-ESPIRO (4.4) NON-1-EN -4-ONA AND INTERMEDIATE PRODUCTS 1-CIANO-1-ACILAMINOCICLOPENTANO. | |
KR910009677A (en) | Method for Preparing Aminotriazine Derivatives | |
KR960004355A (en) | Organosilane containing quaternary ammonium salt and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20090326 Year of fee payment: 8 |
|
LAPS | Lapse due to unpaid annual fee |