Dimethylformamide → 2-Fluoro-3-phenoxybenzaldehyde
Reaction equation
CC1(C)CCCC(C)(C)N1.C([Li])CCC.[C:16]1([O:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[F:29])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.CN(C)[CH:32]=[O:33]>C1COCC1>[F:29][C:24]1[C:23]([O:22][C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=2)=[CH:28][CH:27]=[CH:26][C:25]=1[CH:32]=[O:33]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -78 °C
Procedure
Cool a solution of 2,2,6,6-tetramethylpiperidine (5.1 mL, 30.0 mmol) in THF (40 mL) to −78° C. Add dropwise n-Butyllithium (18.7 mL, 30.0 mmol, 1.6 M in hexanes) and stir for 10 min at −78° C. Add dropwise 2-fluorophenyl phenyl ether (4.7 g, 25.0 mmol), stir 2 h at −78° C. Add N,N-dimethylformamide (2.3 mL, 30.0 mmol) dropwise over 15 min. Stir the resulting mixture for 3 h at −78° C. and allow to warm to ambient temperature over 16 h. Quench the reaction mixture with water (50 mL), extract with ethyl acetate, dry over Na2SO4, filter and concentrate under reduced pressure to give an oil. Crystallize the oil with hexanes to give a solid, collect and recrystallize from hexanes/ethyl acetate/methylene chloride to give the title compound: mp 75–77° C.; MS(m/e): 216 (M+); Calculated for C13H9FO2: Calcd: C, 72.22; H, 4.20. Found: C, 72.41; H, 4.23. Purification of the mother liquors by silica gel chromatography (2–3% ethyl acetate/hexanes) gives an additional amount of the title compound: MS(m/e): 216 (M+).
Workup
- stirringstir 2 h at −78° C
- stirringStir the resulting mixture for 3 h at −78° C.
- temperatureto warm to ambient temperature over 16 h
- customQuench the reaction mixture with water (50 mL)
- extractionextract with ethyl acetate
- dry with materialdry over Na2SO4
- filtrationfilter
- concentrationconcentrate under reduced pressure
- customto give an oil
- customCrystallize the oil with hexanes
- customto give a solid
- customcollect
- customrecrystallize from hexanes/ethyl acetate/methylene chloride
Sources & evidence
- ORD record
- ord-2ab16f4a378c453183d7bd0d4da37541
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07157488B2
Reaction notes
Loading…