CN1119323C - 丙二腈的制备方法 - Google Patents
丙二腈的制备方法 Download PDFInfo
- Publication number
- CN1119323C CN1119323C CN99104071A CN99104071A CN1119323C CN 1119323 C CN1119323 C CN 1119323C CN 99104071 A CN99104071 A CN 99104071A CN 99104071 A CN99104071 A CN 99104071A CN 1119323 C CN1119323 C CN 1119323C
- Authority
- CN
- China
- Prior art keywords
- general formula
- propane dinitrile
- cycloalkyl
- alkyl
- preparation
- 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 - Fee Related
Links
- CUONGYYJJVDODC-UHFFFAOYSA-N malononitrile Chemical compound N#CCC#N CUONGYYJJVDODC-UHFFFAOYSA-N 0.000 title claims abstract description 16
- 238000000034 method Methods 0.000 title claims abstract description 12
- 238000002360 preparation method Methods 0.000 title claims abstract description 6
- 150000002527 isonitriles Chemical class 0.000 claims abstract description 9
- 150000002825 nitriles Chemical class 0.000 claims abstract description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 27
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- ZRKSVHFXTRFQFL-UHFFFAOYSA-N isocyanomethane Chemical compound C[N+]#[C-] ZRKSVHFXTRFQFL-UHFFFAOYSA-N 0.000 claims description 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000007795 chemical reaction product Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- IAQRGUVFOMOMEM-ARJAWSKDSA-N cis-but-2-ene Chemical compound C\C=C/C IAQRGUVFOMOMEM-ARJAWSKDSA-N 0.000 description 3
- IAHFWCOBPZCAEA-UHFFFAOYSA-N succinonitrile Chemical compound N#CCCC#N IAHFWCOBPZCAEA-UHFFFAOYSA-N 0.000 description 3
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 3
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000001149 thermolysis Methods 0.000 description 2
- JJNZXLAFIPKXIG-UHFFFAOYSA-N 2-Chlorobenzylidenemalononitrile Chemical compound ClC1=CC=CC=C1C=C(C#N)C#N JJNZXLAFIPKXIG-UHFFFAOYSA-N 0.000 description 1
- PUXIXZKRDMDACV-UHFFFAOYSA-N C=CC#N.N#CCCC#N Chemical compound C=CC#N.N#CCCC#N PUXIXZKRDMDACV-UHFFFAOYSA-N 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- -1 isobutyl- Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH66598 | 1998-03-19 | ||
| CH0665/1998 | 1998-03-19 | ||
| CH0665/98 | 1998-03-19 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1232819A CN1232819A (zh) | 1999-10-27 |
| CN1119323C true CN1119323C (zh) | 2003-08-27 |
Family
ID=4192289
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN99104071A Expired - Fee Related CN1119323C (zh) | 1998-03-19 | 1999-03-18 | 丙二腈的制备方法 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5959136A (cg-RX-API-DMAC10.html) |
| EP (1) | EP0943605A3 (cg-RX-API-DMAC10.html) |
| JP (1) | JPH11322699A (cg-RX-API-DMAC10.html) |
| KR (1) | KR100618365B1 (cg-RX-API-DMAC10.html) |
| CN (1) | CN1119323C (cg-RX-API-DMAC10.html) |
| CA (1) | CA2263840C (cg-RX-API-DMAC10.html) |
| CZ (1) | CZ84899A3 (cg-RX-API-DMAC10.html) |
| HU (1) | HU223518B1 (cg-RX-API-DMAC10.html) |
| IL (1) | IL128844A (cg-RX-API-DMAC10.html) |
| IN (1) | IN188424B (cg-RX-API-DMAC10.html) |
| PL (1) | PL193541B1 (cg-RX-API-DMAC10.html) |
| RU (1) | RU2225391C2 (cg-RX-API-DMAC10.html) |
| SK (1) | SK34399A3 (cg-RX-API-DMAC10.html) |
| TW (1) | TWI224088B (cg-RX-API-DMAC10.html) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI313676B (en) * | 2002-12-05 | 2009-08-21 | Syngenta Participations Ag | Process for the preparation of phenylmalonic acid dinitriles |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3006492A1 (de) * | 1980-02-21 | 1981-08-27 | Degussa Ag, 6000 Frankfurt | Verfahren zur gewinnung von malonsaeuredinitril |
-
1999
- 1999-03-01 IN IN250MA1999 patent/IN188424B/en unknown
- 1999-03-02 CA CA002263840A patent/CA2263840C/en not_active Expired - Fee Related
- 1999-03-04 IL IL12884499A patent/IL128844A/xx not_active IP Right Cessation
- 1999-03-10 CZ CZ99848A patent/CZ84899A3/cs unknown
- 1999-03-11 EP EP99104840A patent/EP0943605A3/de not_active Withdrawn
- 1999-03-12 KR KR1019990008314A patent/KR100618365B1/ko not_active Expired - Fee Related
- 1999-03-12 SK SK343-99A patent/SK34399A3/sk unknown
- 1999-03-16 TW TW088104018A patent/TWI224088B/zh not_active IP Right Cessation
- 1999-03-16 JP JP11071055A patent/JPH11322699A/ja active Pending
- 1999-03-18 RU RU99105594/04A patent/RU2225391C2/ru not_active IP Right Cessation
- 1999-03-18 PL PL332064A patent/PL193541B1/pl not_active IP Right Cessation
- 1999-03-18 CN CN99104071A patent/CN1119323C/zh not_active Expired - Fee Related
- 1999-03-19 US US09/272,164 patent/US5959136A/en not_active Expired - Fee Related
- 1999-03-19 HU HU9900699A patent/HU223518B1/hu not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| SK34399A3 (en) | 2000-02-14 |
| IN188424B (cg-RX-API-DMAC10.html) | 2002-09-21 |
| IL128844A (en) | 2003-07-06 |
| TWI224088B (en) | 2004-11-21 |
| CN1232819A (zh) | 1999-10-27 |
| PL332064A1 (en) | 1999-09-27 |
| PL193541B1 (pl) | 2007-02-28 |
| IL128844A0 (en) | 2000-01-31 |
| CZ84899A3 (cs) | 1999-10-13 |
| KR19990077832A (ko) | 1999-10-25 |
| JPH11322699A (ja) | 1999-11-24 |
| RU2225391C2 (ru) | 2004-03-10 |
| CA2263840A1 (en) | 1999-09-19 |
| HUP9900699A1 (hu) | 2000-09-28 |
| HK1023108A1 (en) | 2000-09-01 |
| HU9900699D0 (en) | 1999-05-28 |
| EP0943605A2 (de) | 1999-09-22 |
| US5959136A (en) | 1999-09-28 |
| HU223518B1 (hu) | 2004-08-30 |
| KR100618365B1 (ko) | 2006-08-30 |
| EP0943605A3 (de) | 2000-01-19 |
| CA2263840C (en) | 2008-05-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20030827 Termination date: 20100318 |