3-Fluoroaniline → N-(3-fluorophenyl)-3,3-bis(methyloxy)propanamide
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][CH:8]=1)[NH2:5].[CH3:9][O-].[Na+].C[O:13]/[CH:14]=[CH:15]/[C:16]([O:18][CH3:19])=[O:17].[NH4+].[Cl-]>C1(C)C=CC=CC=1.CO.CCOC(C)=O>[F:1][C:2]1[CH:3]=[C:4]([NH:5][C:14](=[O:13])[CH2:15][CH:16]([O:18][CH3:19])[O:17][CH3:9])[CH:6]=[CH:7][CH:8]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Conditions
- Temperature
- 70 °C
Procedure
3-Fluoroaniline (50 g, 450 mmol) was dissolved in toluene (500 ml) and 25% NaOMe in MeOH (120 ml) and methyl (2E)-3-(methyloxy)-2-propenoate (57.4 ml, 495 mmol) were added. The mixture was then heated to 70° C. and stirred at this temperature for 2.5 hours. The solvent was then reduced to around a quarter of the original volume and the reaction was then treated with NH4Cl until pH 7 was reached (approx 500 ml used). EtOAc was added to the reaction and the layers separated, the aqueous layer was then extracted three times with EtOAc and the combined organic layers dried with MgSO4. The solvents were removed and the crude residues were purified by column chromatography on silica gel using a 30-50% EtOAc/40-60 petroleum ether gradient. Fractions containing product were concentrated to afford the desired compound (40.68 g, 40%) and a less pure batch (6.17 g, 6%)
Workup
- customthe layers separated
- extractionthe aqueous layer was then extracted three times with EtOAc
- dry with materialthe combined organic layers dried with MgSO4
- customThe solvents were removed
- customthe crude residues were purified by column chromatography on silica gel using a 30-50% EtOAc/40-60 petroleum ether gradient
- additionFractions containing product
- concentrationwere concentrated
Sources & evidence
- ORD record
- ord-99124118a1434b1ca0fe5d9d7fd52d9c
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08071592B2
Reaction notes
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