Water → HCID 12813906, compound
Reaction equation
N1([C:6]2[CH2:11][CH2:10][CH2:9][CH2:8][CH:7]=2)CCCC1.[CH:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=1)=[CH2:13].[OH2:20]>COCCOCCOC>[N:15]1[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=1[CH2:12][CH2:13][CH:6]1[CH2:7][CH2:8][CH2:9][CH2:10][C:11]1=[O:20]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Example 290 A) A sample of 1-Pyrrolidino-1-cyclohexene (7.1 mL, 44 mmol) and 2-vinylpyridine (4.3 mL, 40 mmol) were refluxed overnight in diglyme (100 mL). Water was then added and the mixture was stirred an additional 2 hours before extracting it with Et2O. The ether layer was dried over MgSO4 and concentrated in vacuo leaving an oil. The residue oil was distilled on a kugelrohr apparatus at 60-80° C. (0.1 mm) to give 2-(2-pyridyl) ethyl-2-cyclohexanone as a yellow oil (6.5 g).
Workup
- extractionbefore extracting it with Et2O
- dry with materialThe ether layer was dried over MgSO4
- concentrationconcentrated in vacuo
- customleaving an oil
- distillationThe residue oil was distilled on a kugelrohr apparatus at 60-80° C. (0.1 mm)
Sources & evidence
- ORD record
- ord-603cd41444ae4920a26c6cf98c5e842e
- Source dataset
- uspto-grants-2000_01
- Patent number
- US06011028
Reaction notes
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