Methanol → 2-n-Hexyl-3-cyanocyclopentanone
Reaction equation
[CH2:1]([C:7]1[C:8](=[O:12])[CH2:9][CH2:10][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].CC(O)([C:16]#[N:17])C.CO.C(=O)([O-])[O-].[Na+].[Na+]>O>[CH2:1]([CH:7]1[CH:11]([C:16]#[N:17])[CH2:10][CH2:9][C:8]1=[O:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 16,6 g of 2-n-hexyl-2-cyclopentenone (see foot note (1) under Table II) 12 g of acetone cyanhydrine (Org. Synth. Coll. Vol.2, p.7), 32 ml of methanol and 0.8 g of sodium carbonate in 12 ml of water, is heated at reflux temperature for 11/2 hours.
Workup
- temperatureis heated
- temperatureat reflux temperature for 11/2 hours
Sources & evidence
- ORD record
- ord-4f08bcffa8c241e1a181feafa240c220
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04016109
Reaction notes
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