DE2209685C3 - Verfahren zur Herstellung von Allylidenphosphoranen - Google Patents
Verfahren zur Herstellung von AllylidenphosphoranenInfo
- Publication number
- DE2209685C3 DE2209685C3 DE2209685A DE2209685A DE2209685C3 DE 2209685 C3 DE2209685 C3 DE 2209685C3 DE 2209685 A DE2209685 A DE 2209685A DE 2209685 A DE2209685 A DE 2209685A DE 2209685 C3 DE2209685 C3 DE 2209685C3
- Authority
- DE
- Germany
- Prior art keywords
- triphenylphosphine
- solution
- ylidene
- trans
- cis
- 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
- 238000000034 method Methods 0.000 title claims description 10
- 238000002360 preparation method Methods 0.000 title claims description 5
- 238000007796 conventional method Methods 0.000 claims 1
- 229910000039 hydrogen halide Inorganic materials 0.000 claims 1
- 239000012433 hydrogen halide Substances 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 150000002902 organometallic compounds Chemical class 0.000 claims 1
- 150000003003 phosphines Chemical group 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 30
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 28
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 19
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 12
- 101150065749 Churc1 gene Proteins 0.000 description 12
- 102100038239 Protein Churchill Human genes 0.000 description 12
- XYDYWTJEGDZLTH-UHFFFAOYSA-N methylenetriphenylphosphorane Chemical group C=1C=CC=CC=1P(C=1C=CC=CC=1)(=C)C1=CC=CC=C1 XYDYWTJEGDZLTH-UHFFFAOYSA-N 0.000 description 11
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 10
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 10
- -1 saturated aliphatic nitriles Chemical class 0.000 description 10
- 238000005160 1H NMR spectroscopy Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- 238000001228 spectrum Methods 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000000921 elemental analysis Methods 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 235000015243 ice cream Nutrition 0.000 description 6
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000004817 gas chromatography Methods 0.000 description 5
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 238000007239 Wittig reaction Methods 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 4
- YPPANBOMPRHASF-UHFFFAOYSA-N (E)-N-[bis(2-methylpropyl)alumanyl]-2-methylpropan-1-imine Chemical compound C(C(C)C)=[N-].C(C(C)C)[Al+]CC(C)C YPPANBOMPRHASF-UHFFFAOYSA-N 0.000 description 3
- ZFFBIQMNKOJDJE-UHFFFAOYSA-N 2-bromo-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(Br)C(=O)C1=CC=CC=C1 ZFFBIQMNKOJDJE-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XJFRUMDEDWVCCN-UHFFFAOYSA-N C(CC)=[N-].C(C(C)C)[Al+]CC(C)C Chemical compound C(CC)=[N-].C(C(C)C)[Al+]CC(C)C XJFRUMDEDWVCCN-UHFFFAOYSA-N 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- YCOZIPAWZNQLMR-UHFFFAOYSA-N heptane - octane Natural products CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004949 mass spectrometry Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 150000002825 nitriles Chemical class 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- QHCSPQISJSEWJE-UHFFFAOYSA-N CC=CC=CCCCCC=CC=CC Chemical compound CC=CC=CCCCCC=CC=CC QHCSPQISJSEWJE-UHFFFAOYSA-N 0.000 description 2
- HSHZSWAKYRHIAP-UHFFFAOYSA-N CC=CC=CCCCCCC=CC=CC Chemical class CC=CC=CCCCCCC=CC=CC HSHZSWAKYRHIAP-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000003462 sulfoxides Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- YRUMHTHCEZRHTN-XAZJVICWSA-N (3E,5Z)-tetradecadienoic acid Chemical compound CCCCCCCC\C=C/C=C/CC(O)=O YRUMHTHCEZRHTN-XAZJVICWSA-N 0.000 description 1
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 1
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 1
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
- OZXIZRZFGJZWBF-UHFFFAOYSA-N 1,3,5-trimethyl-2-(2,4,6-trimethylphenoxy)benzene Chemical compound CC1=CC(C)=CC(C)=C1OC1=C(C)C=C(C)C=C1C OZXIZRZFGJZWBF-UHFFFAOYSA-N 0.000 description 1
- JNYUCBGTSGGRAV-UHFFFAOYSA-N 2,4-dimethylpenta-1,3-dienylbenzene Chemical compound CC(C)=CC(C)=CC1=CC=CC=C1 JNYUCBGTSGGRAV-UHFFFAOYSA-N 0.000 description 1
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 1
- CIVIWCVVOFNUST-VFABXPAXSA-N Bombycol Natural products C(CCCCCCCC\C=C\C=CCCC)O CIVIWCVVOFNUST-VFABXPAXSA-N 0.000 description 1
- BFCXLKKMAJPCGP-UHFFFAOYSA-N CC=CC=CCCCCCCC=CC=CC Chemical compound CC=CC=CCCCCCCC=CC=CC BFCXLKKMAJPCGP-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000002820 allylidene group Chemical group [H]C(=[*])C([H])=C([H])[H] 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- RAVTVJSDZKTXOP-UHFFFAOYSA-N bis(2-methylpropyl)alumanylium butylideneazanide Chemical compound C(CCC)=[N-].C(C(C)C)[Al+]CC(C)C RAVTVJSDZKTXOP-UHFFFAOYSA-N 0.000 description 1
- CIVIWCVVOFNUST-SCFJQAPRSA-N bombykol Chemical compound CCC\C=C/C=C/CCCCCCCCCO CIVIWCVVOFNUST-SCFJQAPRSA-N 0.000 description 1
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229940117916 cinnamic aldehyde Drugs 0.000 description 1
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- DLLJVQNYBYOKGS-UHFFFAOYSA-N ethoxyethane;pentane Chemical compound CCCCC.CCOCC DLLJVQNYBYOKGS-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- AILKHAQXUAOOFU-UHFFFAOYSA-N hexanenitrile Chemical compound CCCCCC#N AILKHAQXUAOOFU-UHFFFAOYSA-N 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000002418 insect attractant Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- LRDFRRGEGBBSRN-UHFFFAOYSA-N isobutyronitrile Chemical compound CC(C)C#N LRDFRRGEGBBSRN-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 1
- CTHWDWZJYNOFSY-UHFFFAOYSA-M methyl-tris(3-methylphenyl)phosphanium;bromide Chemical compound [Br-].CC1=CC=CC([P+](C)(C=2C=C(C)C=CC=2)C=2C=C(C)C=CC=2)=C1 CTHWDWZJYNOFSY-UHFFFAOYSA-M 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- QXOYPGTWWXJFDI-UHFFFAOYSA-N nonanedinitrile Chemical compound N#CCCCCCCCC#N QXOYPGTWWXJFDI-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- BTNXBLUGMAMSSH-UHFFFAOYSA-N octanedinitrile Chemical compound N#CCCCCCCC#N BTNXBLUGMAMSSH-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000003822 preparative gas chromatography Methods 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- LFNXCUNDYSYVJY-UHFFFAOYSA-N tris(3-methylphenyl)phosphane Chemical compound CC1=CC=CC(P(C=2C=C(C)C=CC=2)C=2C=C(C)C=CC=2)=C1 LFNXCUNDYSYVJY-UHFFFAOYSA-N 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27L—REMOVING BARK OR VESTIGES OF BRANCHES; SPLITTING WOOD; MANUFACTURE OF VENEER, WOODEN STICKS, WOOD SHAVINGS, WOOD FIBRES OR WOOD POWDER
- B27L11/00—Manufacture of wood shavings, chips, powder, or the like; Tools therefor
- B27L11/02—Manufacture of wood shavings, chips, powder, or the like; Tools therefor of wood shavings or the like
-
- 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/061—Aluminium compounds with C-aluminium linkage
- C07F5/066—Aluminium compounds with C-aluminium linkage compounds with Al linked to an element other than Al, C, H or halogen (this includes Al-cyanide linkage)
-
- 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
- C07F9/535—Organo-phosphoranes
- C07F9/5352—Phosphoranes containing the structure P=C-
-
- 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
- C07F9/54—Quaternary phosphonium compounds
- C07F9/5428—Acyclic unsaturated phosphonium compounds
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02J—CIRCUIT ARRANGEMENTS OR SYSTEMS FOR SUPPLYING OR DISTRIBUTING ELECTRIC POWER; SYSTEMS FOR STORING ELECTRIC ENERGY
- H02J7/00—Circuit arrangements for charging or depolarising batteries or for supplying loads from batteries
- H02J7/02—Circuit arrangements for charging or depolarising batteries or for supplying loads from batteries for charging batteries from AC mains by converters
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02J—CIRCUIT ARRANGEMENTS OR SYSTEMS FOR SUPPLYING OR DISTRIBUTING ELECTRIC POWER; SYSTEMS FOR STORING ELECTRIC ENERGY
- H02J2207/00—Indexing scheme relating to details of circuit arrangements for charging or depolarising batteries or for supplying loads from batteries
- H02J2207/20—Charging or discharging characterised by the power electronics converter
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Mechanical Engineering (AREA)
- Forests & Forestry (AREA)
- Wood Science & Technology (AREA)
- Manufacturing & Machinery (AREA)
- Toxicology (AREA)
- Power Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2209685A DE2209685C3 (de) | 1972-03-01 | 1972-03-01 | Verfahren zur Herstellung von Allylidenphosphoranen |
| GB826573A GB1408851A (en) | 1972-03-01 | 1973-02-20 | Process for preparing allylidene phosphoranes |
| US335986A US3919325A (en) | 1972-03-01 | 1973-02-26 | Process for preparing allylidenphosphoranes |
| CA164,645A CA989419A (en) | 1972-03-01 | 1973-02-27 | Process for preparing allylidene phosphoranes |
| JP48024229A JPS516134B2 (enExample) | 1972-03-01 | 1973-02-28 | |
| FR7307181A FR2174186B1 (enExample) | 1972-03-01 | 1973-02-28 | |
| CH293473A CH598274A5 (enExample) | 1972-03-01 | 1973-02-28 | |
| IT20975/73A IT979569B (it) | 1972-03-01 | 1973-02-28 | Procedimento per la preparazione di allilidenfosforani |
| AT177573A AT320672B (de) | 1972-03-01 | 1973-02-28 | Verfahren zur Herstellung von Allylidenphosphoranen |
| NL7302822.A NL165466C (nl) | 1972-03-01 | 1973-02-28 | Werkwijze om een bis(triarylfosfin)koolwaterstof te bereiden. |
| BE128237A BE796117A (fr) | 1972-03-01 | 1973-02-28 | Procede pour l'obtention d'allylidenephosphoranes |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2209685A DE2209685C3 (de) | 1972-03-01 | 1972-03-01 | Verfahren zur Herstellung von Allylidenphosphoranen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2209685A1 DE2209685A1 (de) | 1973-09-20 |
| DE2209685B2 DE2209685B2 (de) | 1974-04-04 |
| DE2209685C3 true DE2209685C3 (de) | 1974-11-07 |
Family
ID=5837507
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2209685A Expired DE2209685C3 (de) | 1972-03-01 | 1972-03-01 | Verfahren zur Herstellung von Allylidenphosphoranen |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3919325A (enExample) |
| JP (1) | JPS516134B2 (enExample) |
| AT (1) | AT320672B (enExample) |
| BE (1) | BE796117A (enExample) |
| CA (1) | CA989419A (enExample) |
| CH (1) | CH598274A5 (enExample) |
| DE (1) | DE2209685C3 (enExample) |
| FR (1) | FR2174186B1 (enExample) |
| GB (1) | GB1408851A (enExample) |
| IT (1) | IT979569B (enExample) |
| NL (1) | NL165466C (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2590252B3 (fr) * | 1985-11-19 | 1988-09-09 | Rolland Sa A | Nouveau procede d'obtention d'a-aminonitriles et leurs applications en synthese organique |
| US6455720B1 (en) * | 2000-06-28 | 2002-09-24 | Takasago International Corporation | 2,2(diarlyl)vinylphosphine compound, palladium catalyst thereof, and process for producing arylamine, diaryl, or arylalkyne with the catalyst |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL98592C (enExample) * | 1957-07-12 | |||
| NL252912A (enExample) * | 1959-06-23 | |||
| US3095454A (en) * | 1961-11-29 | 1963-06-25 | Monsanto Chemicals | Triarylphosphinedihalomethylenes |
| US3247266A (en) * | 1962-02-12 | 1966-04-19 | Monsanto Co | 1, 1-dihaloolefins |
| US3647856A (en) * | 1967-12-08 | 1972-03-07 | Du Pont | Sulfinyl ylids |
| US3723537A (en) * | 1968-06-15 | 1973-03-27 | Basf Ag | Process for preparing alkylidene phosphoranes |
-
1972
- 1972-03-01 DE DE2209685A patent/DE2209685C3/de not_active Expired
-
1973
- 1973-02-20 GB GB826573A patent/GB1408851A/en not_active Expired
- 1973-02-26 US US335986A patent/US3919325A/en not_active Expired - Lifetime
- 1973-02-27 CA CA164,645A patent/CA989419A/en not_active Expired
- 1973-02-28 IT IT20975/73A patent/IT979569B/it active
- 1973-02-28 FR FR7307181A patent/FR2174186B1/fr not_active Expired
- 1973-02-28 AT AT177573A patent/AT320672B/de not_active IP Right Cessation
- 1973-02-28 CH CH293473A patent/CH598274A5/xx not_active IP Right Cessation
- 1973-02-28 JP JP48024229A patent/JPS516134B2/ja not_active Expired
- 1973-02-28 BE BE128237A patent/BE796117A/xx not_active IP Right Cessation
- 1973-02-28 NL NL7302822.A patent/NL165466C/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| NL165466C (nl) | 1981-04-15 |
| GB1408851A (en) | 1975-10-08 |
| NL165466B (nl) | 1980-11-17 |
| AT320672B (de) | 1975-02-25 |
| CA989419A (en) | 1976-05-18 |
| DE2209685A1 (de) | 1973-09-20 |
| NL7302822A (enExample) | 1973-09-04 |
| BE796117A (fr) | 1973-08-28 |
| FR2174186B1 (enExample) | 1976-09-10 |
| FR2174186A1 (enExample) | 1973-10-12 |
| IT979569B (it) | 1974-09-30 |
| US3919325A (en) | 1975-11-11 |
| CH598274A5 (enExample) | 1978-04-28 |
| JPS516134B2 (enExample) | 1976-02-25 |
| JPS4899148A (enExample) | 1973-12-15 |
| ATA177574A (de) | 1976-01-15 |
| DE2209685B2 (de) | 1974-04-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| E77 | Valid patent as to the heymanns-index 1977 | ||
| 8339 | Ceased/non-payment of the annual fee |