PL115880B2 - Process for preparing /e/-1-/2,3,3-trimethylcyclopen-1-enyl/-pent-3-en-2-one - Google Patents
Process for preparing /e/-1-/2,3,3-trimethylcyclopen-1-enyl/-pent-3-en-2-one Download PDFInfo
- Publication number
- PL115880B2 PL115880B2 PL21908779A PL21908779A PL115880B2 PL 115880 B2 PL115880 B2 PL 115880B2 PL 21908779 A PL21908779 A PL 21908779A PL 21908779 A PL21908779 A PL 21908779A PL 115880 B2 PL115880 B2 PL 115880B2
- Authority
- PL
- Poland
- Prior art keywords
- trimethylcyclopenten
- trimethylcyclopen
- pent
- enyl
- preparing
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims 3
- -1 2,3,3-trimethylcyclopenten-1-yl Chemical group 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- PBAKTNCSUCNJRE-UHFFFAOYSA-N 2-(2,3,3-trimethylcyclopenten-1-yl)acetonitrile Chemical compound CC1=C(CC#N)CCC1(C)C PBAKTNCSUCNJRE-UHFFFAOYSA-N 0.000 claims 2
- 238000003747 Grignard reaction Methods 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 150000004820 halides Chemical class 0.000 claims 1
- 238000006317 isomerization reaction Methods 0.000 claims 1
- 150000003138 primary alcohols Chemical class 0.000 claims 1
- 150000003510 tertiary aliphatic amines Chemical class 0.000 claims 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Claims (3)
- Zastrzezenia patentowe 1. Sposób wytwarzania /E/-l-/2,3,3-trójmetylocyklopenten-l- ylo/-penten-3-onu-2, o wzorze przedstawio¬ nym na rysunku, znamienny tym, ze 2,3,3-trójmetylocyklopenten- 1-yloacetonitrl poddaje sie reakcji Grignarda z halogenkiem allilomagnezowym, a nastepnie poddaje sie izomeryzacji wobec katalizatorów zasado¬ wych.
- 2. Sposób wedlug zastrz. 1, znamienny tym, ze proces izomeryzacji prowadzi sie w srodowisku alkoholu pierwszorzedowego, stosujac jako katalizator trzeciorzedowa amine alifatyczna.
- 3. Sposób wytwarzania /E/-l-/2,3,3-trójmetylocyklopenten-l-ylo/ -penten-3-onu-2, o wzorze przedstawio¬ nym na rysunku, znamienny tym, ze 2,3,3-trójmetylocyklopenten-l-yloacetonitryl poddaje sie reakcji Grignarda z halogenkiem 1-propenylomagnezowym. Prac. Poligraf. UP PRL naklad 120+18 Cena 45 zl PL
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL21908779A PL115880B2 (en) | 1979-10-20 | 1979-10-20 | Process for preparing /e/-1-/2,3,3-trimethylcyclopen-1-enyl/-pent-3-en-2-one |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL21908779A PL115880B2 (en) | 1979-10-20 | 1979-10-20 | Process for preparing /e/-1-/2,3,3-trimethylcyclopen-1-enyl/-pent-3-en-2-one |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| PL219087A2 PL219087A2 (pl) | 1980-08-25 |
| PL115880B2 true PL115880B2 (en) | 1981-05-30 |
Family
ID=19999004
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL21908779A PL115880B2 (en) | 1979-10-20 | 1979-10-20 | Process for preparing /e/-1-/2,3,3-trimethylcyclopen-1-enyl/-pent-3-en-2-one |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL115880B2 (pl) |
-
1979
- 1979-10-20 PL PL21908779A patent/PL115880B2/pl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PL219087A2 (pl) | 1980-08-25 |
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