JPH032190A - 第２酸化ホスフアンの製法 - Google Patents
第２酸化ホスフアンの製法Info
- Publication number
- JPH032190A JPH032190A JP18760089A JP18760089A JPH032190A JP H032190 A JPH032190 A JP H032190A JP 18760089 A JP18760089 A JP 18760089A JP 18760089 A JP18760089 A JP 18760089A JP H032190 A JPH032190 A JP H032190A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- phosphane
- oxide
- phosphonic acid
- tetrahydrofuran
- 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.)
- Granted
Links
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical group [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 title claims description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims abstract description 30
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims abstract description 15
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000005922 Phosphane Substances 0.000 claims abstract description 5
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims abstract description 5
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims abstract description 5
- 229910000064 phosphane Inorganic materials 0.000 claims abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 239000008346 aqueous phase Substances 0.000 claims description 7
- 239000000706 filtrate Substances 0.000 claims description 6
- 239000012074 organic phase Substances 0.000 claims description 6
- 239000012071 phase Substances 0.000 claims description 6
- 230000007062 hydrolysis Effects 0.000 claims description 5
- 238000006460 hydrolysis reaction Methods 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- 239000011777 magnesium Substances 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 230000003472 neutralizing effect Effects 0.000 claims description 4
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 230000002209 hydrophobic effect Effects 0.000 claims description 2
- 238000006386 neutralization reaction Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- -1 phosphane dioxide Chemical compound 0.000 claims 1
- 239000004615 ingredient Substances 0.000 abstract 3
- 239000007818 Grignard reagent Substances 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000004079 fireproofing Methods 0.000 abstract 1
- 150000004795 grignard reagents Chemical class 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- VCUVETGKTILCLC-UHFFFAOYSA-N 5,5-dimethyl-1-pyrroline N-oxide Chemical compound CC1(C)CCC=[N+]1[O-] VCUVETGKTILCLC-UHFFFAOYSA-N 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- YFPJFKYCVYXDJK-UHFFFAOYSA-N Diphenylphosphine oxide Chemical compound C=1C=CC=CC=1[P+](=O)C1=CC=CC=C1 YFPJFKYCVYXDJK-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- MXBDBLBKBBAYGD-UHFFFAOYSA-N P(O)(O)=O.C Chemical compound P(O)(O)=O.C MXBDBLBKBBAYGD-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- GOJNABIZVJCYFL-UHFFFAOYSA-M dimethylphosphinate Chemical compound CP(C)([O-])=O GOJNABIZVJCYFL-UHFFFAOYSA-M 0.000 description 2
- LRMLWYXJORUTBG-UHFFFAOYSA-N dimethylphosphorylmethane Chemical compound CP(C)(C)=O LRMLWYXJORUTBG-UHFFFAOYSA-N 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- CCERQOYLJJULMD-UHFFFAOYSA-M magnesium;carbanide;chloride Chemical compound [CH3-].[Mg+2].[Cl-] CCERQOYLJJULMD-UHFFFAOYSA-M 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- WSEDDYVBLJDHPD-UHFFFAOYSA-N methyl(3-methylbutoxy)phosphinic acid Chemical compound CC(C)CCOP(C)(O)=O WSEDDYVBLJDHPD-UHFFFAOYSA-N 0.000 description 2
- YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical compound CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- UFGGBJYMEZXRLU-UHFFFAOYSA-N 1-methylphosphonoylethane Chemical compound CCP(C)=O UFGGBJYMEZXRLU-UHFFFAOYSA-N 0.000 description 1
- FGOJCPKOOGIRPA-UHFFFAOYSA-N 1-o-tert-butyl 4-o-ethyl 5-oxoazepane-1,4-dicarboxylate Chemical compound CCOC(=O)C1CCN(C(=O)OC(C)(C)C)CCC1=O FGOJCPKOOGIRPA-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- GATNOFPXSDHULC-UHFFFAOYSA-N ethylphosphonic acid Chemical compound CCP(O)(O)=O GATNOFPXSDHULC-UHFFFAOYSA-N 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000013462 industrial intermediate Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- IWCVDCOJSPWGRW-UHFFFAOYSA-M magnesium;benzene;chloride Chemical compound [Mg+2].[Cl-].C1=CC=[C-]C=C1 IWCVDCOJSPWGRW-UHFFFAOYSA-M 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000010626 work up procedure Methods 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/46—Phosphinous acids [R2POH], [R2P(= O)H]: Thiophosphinous acids including[R2PSH]; [R2P(=S)H]; Aminophosphines [R2PNH2]; Derivatives 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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3824776.3 | 1988-07-21 | ||
| DE19883824776 DE3824776A1 (de) | 1988-07-21 | 1988-07-21 | Verfahren zur herstellung von sekundaeren phosphanoxiden |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH032190A true JPH032190A (ja) | 1991-01-08 |
| JPH0555515B2 JPH0555515B2 (en, 2012) | 1993-08-17 |
Family
ID=6359215
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18760089A Granted JPH032190A (ja) | 1988-07-21 | 1989-07-21 | 第２酸化ホスフアンの製法 |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0351548A3 (en, 2012) |
| JP (1) | JPH032190A (en, 2012) |
| DE (1) | DE3824776A1 (en, 2012) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008032531A1 (fr) * | 2006-09-13 | 2008-03-20 | National Institute Of Advanced Industrial Science And Technology | Procédé pour la production d'un composé du phosphore optiquement actif |
| JP2011162485A (ja) * | 2010-02-10 | 2011-08-25 | National Institute Of Advanced Industrial Science & Technology | 光学活性リン化合物の製造方法 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9104050D0 (en) * | 1991-02-27 | 1991-04-17 | Ciba Geigy Ag | Compounds |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3521770C2 (de) * | 1984-06-28 | 1993-10-21 | Basf Ag | Verfahren zur Herstellung von Diarylalkoxyphosphinen |
-
1988
- 1988-07-21 DE DE19883824776 patent/DE3824776A1/de not_active Withdrawn
-
1989
- 1989-06-14 EP EP19890110742 patent/EP0351548A3/de not_active Withdrawn
- 1989-07-21 JP JP18760089A patent/JPH032190A/ja active Granted
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008032531A1 (fr) * | 2006-09-13 | 2008-03-20 | National Institute Of Advanced Industrial Science And Technology | Procédé pour la production d'un composé du phosphore optiquement actif |
| JP2008069103A (ja) * | 2006-09-13 | 2008-03-27 | National Institute Of Advanced Industrial & Technology | 光学活性リン化合物の製造方法 |
| JP2011162485A (ja) * | 2010-02-10 | 2011-08-25 | National Institute Of Advanced Industrial Science & Technology | 光学活性リン化合物の製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE3824776A1 (de) | 1990-01-25 |
| EP0351548A3 (de) | 1991-01-16 |
| EP0351548A2 (de) | 1990-01-24 |
| JPH0555515B2 (en, 2012) | 1993-08-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6359171B1 (en) | Process for preparing dialkylphosphinic acids and their salts | |
| US4083898A (en) | Process for preparing O-aryl, N-phosphonomethylglycinonitriles | |
| JP2002308890A (ja) | エタンビス（アルキルホスフィン）酸類の製造方法 | |
| Oleksyszyn et al. | New phosphonic analogs of aspartic and glutamic acid by aminoalkylation of trivalent phosphorus chlorides with ethyl acetyloacetate or ethyl levulinate and benzyl carbamate | |
| US3959361A (en) | Process of producing amino methylene phosphonic acids | |
| US4332746A (en) | Diphosphonodicarboxylic acid esters | |
| JPH032190A (ja) | 第２酸化ホスフアンの製法 | |
| US6388125B1 (en) | Process for preparing phosphinic acids | |
| WO2000014093A1 (en) | Synthesis of phosphonomethyliminodiacetic acid with reduced effluent | |
| EP0097522A2 (en) | Preparation of N-phosphonomethylglycine | |
| Maier et al. | ORGANIC PHOSPHORUS COMPOUNDS 771 SYNTHESIS AND PROPERTIES OF PHOSPHINOTHRICIN HOMOLOGS AND ANALOGS | |
| JPH03181493A (ja) | 純粋な環状リン酸ジアリールエステルの製造方法 | |
| JPS5918400B2 (ja) | ホスホン酸エステル | |
| JP3111076B2 (ja) | アミノメタンホスホン酸およびアミノメチル―ホスフィン酸の製造方法 | |
| Mikroyannidis | Hydroxy and/or carboxy substituted phosphonic and bisphosphonic acids usable as corrosion and scale inhibitors | |
| JP2000355596A (ja) | アルキル亜ホスホン酸エステルの製造方法 | |
| US4988489A (en) | Recovery of phosphorus values from waste phosphoric acid liquors | |
| JPS63122694A (ja) | ２−アミノ−４−ホスフイニルブタン酸の製造法 | |
| US3222378A (en) | Phthalimidomethyl phosphorus compounds | |
| US20040236144A1 (en) | Method for producing $g(a)-aminophosphonic acids | |
| US2802854A (en) | Method of preparing phosphoric acid esters of diethylstilbestrol | |
| JPS5926633B2 (ja) | 燐含有エステルの製造法 | |
| US4032603A (en) | Production of phosphorus oxy compounds | |
| US4966991A (en) | Process for the preparation of alkali metal phosphonoformates | |
| US5157153A (en) | Preparation of phosphinoacetic acids |