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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide

α-Cyclogeranonitrile synthesis

14synthesis methods
3,7-Dimethyl-2,6-octadienenitrile

5146-66-7
139 suppliers
$14.00/1mL

57524-14-8 Synthesis
2,6,6-TRIMETHYLCYCLOHEX-2-ENE-1-YLCARBONITRILE

57524-14-8
12 suppliers
inquiry

α-Cyclogeranonitrile

57524-13-7
9 suppliers
inquiry

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Yield:57524-13-7 86%

Reaction Conditions:

with sulfuric acid in nitromethane at 0; for 0.5 h;Title compound not separated from byproducts.;Cyclization;

References:

Jansen, Frans Jos H. M.;Lugtenburg, Johan [European Journal of Organic Chemistry,2000,# 5,p. 829 - 836]

5585-39-7 Synthesis
(E)-3,7-Dimethyl-2,6-octadienenitrile

5585-39-7
17 suppliers
inquiry

α-Cyclogeranonitrile

57524-13-7
9 suppliers
inquiry

References
3,7-Dimethyl-2,6-octadienenitrile

5146-66-7
139 suppliers
$14.00/1mL

α-Cyclogeranonitrile

57524-13-7
9 suppliers
inquiry

References
6-Methyl-5-hepten-2-one

110-93-0
298 suppliers
$8.00/25g

α-Cyclogeranonitrile

57524-13-7
9 suppliers
inquiry

References
3,7-Dimethyl-2,6-octadienenitrile

5146-66-7
139 suppliers
$14.00/1mL

57524-14-8 Synthesis
2,6,6-TRIMETHYLCYCLOHEX-2-ENE-1-YLCARBONITRILE

57524-14-8
12 suppliers
inquiry

α-Cyclogeranonitrile

57524-13-7
9 suppliers
inquiry

Cyclohexanecarbonitrile, 2,2-dimethyl-6-methylene-

140848-05-1
0 suppliers
inquiry

References