Benzaldehyde → HCID 712329, compound
Reaction equation
[N:1]12[CH2:8][CH2:7][CH:4]([CH2:5][CH2:6]1)[C:3](=[O:9])[CH2:2]2.[CH:10](=O)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[OH-].[Na+]>C(O)C>[CH:10](=[C:2]1/[N:1]2[CH2:8][CH2:7][CH:4]([C:3]/1=[O:9])[CH2:5][CH2:6]2)/[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3-quinuclidinone (20.9 g, 167 mmol), benzaldehyde (17.7 g, 167 mmol), and one pellet of sodium hydroxide in 75 mL of ethanol was refluxed for 1.5 h. After the solution was cooled, the yellow precipitates were collected, washed with ethanol, and dried to give (Z)-2-benzylidenequinuclidin-3-one (32.5 g, yield: 91.2%, mp 130-132° C.).
Workup
- temperaturewas refluxed for 1.5 h
- temperatureAfter the solution was cooled
- customthe yellow precipitates
- customwere collected
- washwashed with ethanol
- customdried
Sources & evidence
- ORD record
- ord-eaa0b2182d3a45bf86e1d4bdbf779d58
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08809364B2
Reaction notes
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