SK6012000A3 - Stable chiral aminobutyronitrile composition - Google Patents
Stable chiral aminobutyronitrile composition Download PDFInfo
- Publication number
- SK6012000A3 SK6012000A3 SK601-2000A SK6012000A SK6012000A3 SK 6012000 A3 SK6012000 A3 SK 6012000A3 SK 6012000 A SK6012000 A SK 6012000A SK 6012000 A3 SK6012000 A3 SK 6012000A3
- Authority
- SK
- Slovakia
- Prior art keywords
- amino
- dimethylbutyronitrile
- composition
- solvent
- stable
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 31
- DQQIUVCNBOJDGF-UHFFFAOYSA-N 2-aminobutanenitrile Chemical compound CCC(N)C#N DQQIUVCNBOJDGF-UHFFFAOYSA-N 0.000 title description 3
- CAOHBROWLMCZRP-LURJTMIESA-N (2r)-2-amino-2,3-dimethylbutanenitrile Chemical compound CC(C)[C@@](C)(N)C#N CAOHBROWLMCZRP-LURJTMIESA-N 0.000 claims abstract description 17
- 239000012454 non-polar solvent Substances 0.000 claims abstract description 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 35
- 239000002904 solvent Substances 0.000 claims description 12
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- 150000008282 halocarbons Chemical class 0.000 claims description 2
- 229930195733 hydrocarbon Chemical class 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 9
- 239000013543 active substance Substances 0.000 abstract description 4
- 239000000243 solution Substances 0.000 description 15
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 238000011156 evaluation Methods 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 7
- 230000006340 racemization Effects 0.000 description 7
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 230000000855 fungicidal effect Effects 0.000 description 4
- 230000002363 herbicidal effect Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 239000002798 polar solvent Substances 0.000 description 3
- 239000012085 test solution Substances 0.000 description 3
- -1 (R) 2-amino-2,3-dimethylbutyronitrile (2S, 3S) tartaric acid salt Chemical class 0.000 description 2
- SXERGJJQSKIUIC-UHFFFAOYSA-N 2-Phenoxypropionic acid Chemical class OC(=O)C(C)OC1=CC=CC=C1 SXERGJJQSKIUIC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000004296 chiral HPLC Methods 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- BTANRVKWQNVYAZ-BYPYZUCNSA-N (2S)-butan-2-ol Chemical compound CC[C@H](C)O BTANRVKWQNVYAZ-BYPYZUCNSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- CAOHBROWLMCZRP-UHFFFAOYSA-N 2-amino-2,3-dimethylbutanenitrile Chemical compound CC(C)C(C)(N)C#N CAOHBROWLMCZRP-UHFFFAOYSA-N 0.000 description 1
- IPEMCIBPDYCJLO-UHFFFAOYSA-N 5-[(3,5,5,8,8-pentamethyl-6,7-dihydronaphthalen-2-yl)methyl]-n-(2,4,6-trimethoxyphenyl)furan-2-carboxamide Chemical compound COC1=CC(OC)=CC(OC)=C1NC(=O)C(O1)=CC=C1CC1=CC(C(CCC2(C)C)(C)C)=C2C=C1C IPEMCIBPDYCJLO-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical class CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- SZRUMHWRJNVJJC-UHFFFAOYSA-N chlorobenzene;1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1.ClC1=CC=CC=C1Cl SZRUMHWRJNVJJC-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 150000004816 dichlorobenzenes Chemical class 0.000 description 1
- 231100000676 disease causative agent Toxicity 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229940017219 methyl propionate Drugs 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/24—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US30385099A | 1999-05-03 | 1999-05-03 | |
| US30440199A | 1999-05-03 | 1999-05-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK6012000A3 true SK6012000A3 (en) | 2001-01-18 |
Family
ID=26973684
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK601-2000A SK6012000A3 (en) | 1999-05-03 | 2000-04-26 | Stable chiral aminobutyronitrile composition |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP1050529B1 (fr) |
| JP (1) | JP2000319112A (fr) |
| KR (1) | KR20000077121A (fr) |
| CN (1) | CN1272313A (fr) |
| AR (1) | AR023938A1 (fr) |
| AT (1) | ATE252549T1 (fr) |
| AU (1) | AU3024500A (fr) |
| BR (1) | BR0002074A (fr) |
| CA (1) | CA2307392A1 (fr) |
| DE (1) | DE60006028D1 (fr) |
| HU (1) | HUP0001711A3 (fr) |
| IL (1) | IL135796A0 (fr) |
| MX (1) | MXPA00004112A (fr) |
| NZ (1) | NZ504199A (fr) |
| PL (1) | PL339972A1 (fr) |
| SK (1) | SK6012000A3 (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60311510T2 (de) * | 2002-11-21 | 2007-10-31 | Dsm Ip Assets B.V. | Verfahren zur racemisierung enantiomerangereicherter alpha-aminonitrile |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4683324A (en) * | 1982-05-25 | 1987-07-28 | American Cyanamid Company | Process for the resolution of certain racemic amino nitriles |
| DE3474815D1 (en) * | 1983-03-28 | 1988-12-01 | American Cyanamid Co | Novel process for the preparation of aminonitriles useful for the preparation of herbicides |
-
2000
- 2000-04-24 IL IL13579600A patent/IL135796A0/xx unknown
- 2000-04-25 JP JP2000123933A patent/JP2000319112A/ja active Pending
- 2000-04-26 SK SK601-2000A patent/SK6012000A3/sk unknown
- 2000-04-27 MX MXPA00004112A patent/MXPA00004112A/es unknown
- 2000-04-27 NZ NZ504199A patent/NZ504199A/en unknown
- 2000-04-27 CN CN00108178A patent/CN1272313A/zh active Pending
- 2000-04-28 EP EP00303586A patent/EP1050529B1/fr not_active Expired - Lifetime
- 2000-04-28 AT AT00303586T patent/ATE252549T1/de not_active IP Right Cessation
- 2000-04-28 PL PL00339972A patent/PL339972A1/xx unknown
- 2000-04-28 DE DE60006028T patent/DE60006028D1/de not_active Expired - Lifetime
- 2000-05-01 KR KR1020000023244A patent/KR20000077121A/ko not_active Withdrawn
- 2000-05-01 CA CA002307392A patent/CA2307392A1/fr not_active Abandoned
- 2000-05-02 BR BR0002074-5A patent/BR0002074A/pt not_active IP Right Cessation
- 2000-05-02 AR ARP000102093A patent/AR023938A1/es not_active Application Discontinuation
- 2000-05-02 AU AU30245/00A patent/AU3024500A/en not_active Abandoned
- 2000-05-02 HU HU0001711A patent/HUP0001711A3/hu unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATE252549T1 (de) | 2003-11-15 |
| EP1050529A3 (fr) | 2001-07-18 |
| AR023938A1 (es) | 2002-09-04 |
| BR0002074A (pt) | 2001-01-02 |
| EP1050529A2 (fr) | 2000-11-08 |
| HU0001711D0 (en) | 2000-06-28 |
| CN1272313A (zh) | 2000-11-08 |
| HUP0001711A2 (hu) | 2001-05-28 |
| MXPA00004112A (es) | 2002-03-08 |
| JP2000319112A (ja) | 2000-11-21 |
| CA2307392A1 (fr) | 2000-11-03 |
| AU3024500A (en) | 2000-11-09 |
| EP1050529B1 (fr) | 2003-10-22 |
| HUP0001711A3 (en) | 2002-12-28 |
| IL135796A0 (en) | 2001-05-20 |
| NZ504199A (en) | 2001-12-21 |
| DE60006028D1 (de) | 2003-11-27 |
| PL339972A1 (en) | 2000-11-06 |
| KR20000077121A (ko) | 2000-12-26 |
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