Dimethylformamide → 1533440-50-4
Reaction equation
Br[C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[CH:11]1[CH2:13][CH2:12]1)[C:5]([OH:7])=[O:6].[Li]CCCC.CN(C)[CH:21]=[O:22]>O1CCCC1.CCOCC>[CH:11]1([C:10]2[CH:9]=[CH:8][C:4]([C:5]([OH:7])=[O:6])=[CH:3][C:2]=2[CH:21]=[O:22])[CH2:13][CH2:12]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -78 °C
Procedure
Into a 100-mL three neck round-bottom flask, which was purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 3-bromo-4-cyclopropylbenzoic acid (compound 10.3, 500 mg, 2.07 mmol) in tetrahydrofuran/Et2O (1:1, 20 mL). The solution was cooled to −78° C. then n-BuLi (2.5 M in THF) (1.8 mL, 4.5 mmol) was added drop-wise with stirring. The resulting solution was stirred for an additional 30 min at −78° C., then N,N-dimethylformamide (0.49 mL, 6.3 mmol) was added drop-wise over 10 min. The mixture was stirred for 2 h at −78° C., then quenched with water (100 mL). The pH of the solution was adjusted to 3-4 with aqueous HCl (6 M), then extracted with ethyl acetate (3×30 mL). The combined organic layers were washed with brine (3×30 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with ethyl acetate/petroleum ether (1:5) as the eluent to yield 0.3 g (76%) of the title compound as a white solid.
Workup
- customInto a 100-mL three neck round-bottom flask, which was purged
- temperaturemaintained with an inert atmosphere of nitrogen
- stirringThe resulting solution was stirred for an additional 30 min at −78° C.
- stirringThe mixture was stirred for 2 h at −78° C.
- customquenched with water (100 mL)
- extractionextracted with ethyl acetate (3×30 mL)
- washThe combined organic layers were washed with brine (3×30 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue was purified by silica gel column chromatography with ethyl acetate/petroleum ether (1:5) as the eluent
Sources & evidence
- ORD record
- ord-dcb4a0592d134a6896c553eb720c25a8
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09428502B2
Reaction notes
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