Acetaldehyde → HCID 19030393, compound
Reaction equation
[CH:1](=O)[CH3:2].[CH:4]1([NH2:11])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1.[OH-].[K+]>>[CH:1](=[N:11][CH:4]1[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1)[CH3:2]Participants
4
Procedure
90% Acetaldehyde (19.55 g) was added dropwise to cycloheptylamine (45.28 g) with ice bath cooling over about 2 hours. After the completion of the dropwise addition, potassium hydroxide, in solid form, was added and the organic layer was separated by a separatory funnel. This liquid was distilled under reduced pressure to obtain pure N-ethylidenecycloheptylamine (47.92 g). b.p. 100°-104° C./106.4 mbar.
Workup
- temperaturecooling over about 2 hours
- additionin solid form, was added
- customthe organic layer was separated by a separatory funnel
- distillationThis liquid was distilled under reduced pressure
Sources & evidence
- ORD record
- ord-66d9127fc0e74cae8759e00507d6c7c9
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05652198
Reaction notes
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