GB887411A - Preparation of ª-, ª--disubstituted-ª--cyanoketones - Google Patents
Preparation of ª-, ª--disubstituted-ª--cyanoketonesInfo
- Publication number
- GB887411A GB887411A GB16587/58A GB1658758A GB887411A GB 887411 A GB887411 A GB 887411A GB 16587/58 A GB16587/58 A GB 16587/58A GB 1658758 A GB1658758 A GB 1658758A GB 887411 A GB887411 A GB 887411A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- ethyl
- formula
- disubstituted
- reaction
- 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
- 150000002576 ketones Chemical class 0.000 abstract 5
- 239000003054 catalyst Substances 0.000 abstract 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 abstract 3
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 abstract 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- FILVIKOEJGORQS-UHFFFAOYSA-N 1,5-dimethylpyrrolidin-2-one Chemical compound CC1CCC(=O)N1C FILVIKOEJGORQS-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 abstract 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 150000001342 alkaline earth metals Chemical class 0.000 abstract 1
- 150000004703 alkoxides Chemical class 0.000 abstract 1
- 239000002585 base Substances 0.000 abstract 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- GTBRTGPZZALPNS-MXHVRSFHSA-N cyanoketone Chemical compound C1C=C2C(C)(C)C(=O)[C@H](C#N)C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@](C)(O)[C@@]1(C)CC2 GTBRTGPZZALPNS-MXHVRSFHSA-N 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 238000005669 hydrocyanation reaction Methods 0.000 abstract 1
- 150000004679 hydroxides Chemical class 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 230000000749 insecticidal effect Effects 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- -1 oxides Chemical class 0.000 abstract 1
- 150000002978 peroxides Chemical class 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US887411XA | 1957-05-31 | 1957-05-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB887411A true GB887411A (en) | 1962-01-17 |
Family
ID=22213172
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB16587/58A Expired GB887411A (en) | 1957-05-31 | 1958-05-23 | Preparation of ª-, ª--disubstituted-ª--cyanoketones |
| GB16702/58A Expired GB887413A (en) | 1957-05-31 | 1958-05-23 | Carbocyclic cyanoketones |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB16702/58A Expired GB887413A (en) | 1957-05-31 | 1958-05-23 | Carbocyclic cyanoketones |
Country Status (2)
| Country | Link |
|---|---|
| BE (1) | BE568220A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
| GB (2) | GB887411A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4788318A (en) * | 1986-11-26 | 1988-11-29 | Huls Aktiengesellschaft | Process for the production of 4,4,8,8,10-pentamethyl-10-cyano-bicyclo[4.4.0]-dec-1,6-en-2-one |
| US6822110B2 (en) | 2002-11-07 | 2004-11-23 | Basf Aktiengesellschaft | CaO-catalyzed preparation of isophoronenitrile |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04279559A (ja) * | 1991-03-05 | 1992-10-05 | Nippo Kagaku Kk | ３−シアノ−３，５，５−トリメチルシクロヘキサノンの製造方法 |
| DE4203456A1 (de) * | 1992-02-07 | 1993-08-12 | Basf Ag | Verfahren zur kontinuierlichen herstellung von 3-cyano-3,5,5-trimethylcyclohexanon |
| CN101851178B (zh) * | 2010-06-01 | 2014-08-06 | 四川省天然气化工研究院 | 异佛尔酮腈的制备方法 |
| DE102011077681A1 (de) * | 2011-06-17 | 2012-12-20 | Evonik Degussa Gmbh | Verfahren zur Herstellung von 3-Cyano-3,5,5-trimethylcyclohexanon |
-
0
- BE BE568220D patent/BE568220A/xx unknown
-
1958
- 1958-05-23 GB GB16587/58A patent/GB887411A/en not_active Expired
- 1958-05-23 GB GB16702/58A patent/GB887413A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4788318A (en) * | 1986-11-26 | 1988-11-29 | Huls Aktiengesellschaft | Process for the production of 4,4,8,8,10-pentamethyl-10-cyano-bicyclo[4.4.0]-dec-1,6-en-2-one |
| US6822110B2 (en) | 2002-11-07 | 2004-11-23 | Basf Aktiengesellschaft | CaO-catalyzed preparation of isophoronenitrile |
Also Published As
| Publication number | Publication date |
|---|---|
| BE568220A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| GB887413A (en) | 1962-01-17 |
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