Phenylacetone → HCID 1488370, compound
Reaction equation
[C:1]1([CH2:7][C:8](=[O:10])[CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:11][N:12]([CH:14](OC)OC)[CH3:13]>CN(C=O)C>[CH3:11][N:12]([CH3:14])/[CH:13]=[C:7](\[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)/[C:8](=[O:10])[CH3:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1-phenylpropan-2-one (2.3 g, 20 mmol) and DMF-DMA (2.4 g, 20 mmol) in DMF (10 mL) was stirred at 100° C. overnight. The reaction mixture was cooled, concentrated, and purified by silica gel column (PE/EtOAc=4:1˜2:1) to give the title compound (0.7 g, 18%) as a yellow oil.
Workup
- temperatureThe reaction mixture was cooled
- concentrationconcentrated
- custompurified by silica gel column (PE/EtOAc=4:1˜2:1)
Sources & evidence
- ORD record
- ord-c5f97dcb40234a7795d545835205264f
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987461B2
Reaction notes
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