Dimethylformamide → (E)-3-Dimethylamino-1-phenyl-propenone
Reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)(=[O:3])[CH3:2].[CH3:10][N:11]([CH:13]=O)[CH3:12]>CC(N(C)C)=O>[CH3:10][N:11]([CH3:13])/[CH:12]=[CH:2]/[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)=[O:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of acetophenone (8.0 g, 66.58 mmol, 1.0 eq) and DMF (5.8 g, 79.90 mmol, 1.2 eq.) in 10.0 mL of DMA in a 25-mL microwave vial was irradiated at 115° C. for 0.5-1 h. The crude reaction mixture was triturated with n-hexane, and the resultant solid was filtered to afford the title compound as a pale yellow solid (3.4 g. 29.3% yield). [M+H] Calc'd for C11H13NO, 176; Found, 176.
Workup
- customwas irradiated at 115° C. for 0.5-1 h
- customThe crude reaction mixture
- customwas triturated with n-hexane
- filtrationthe resultant solid was filtered
Sources & evidence
- ORD record
- ord-371159a2e5384078b86cfea8300c6367
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987461B2
Reaction notes
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