Potassium Carbonate → HCID 52466667, compound
Reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[N+:9]([O-:11])=[O:10].[OH:12][C:13]1[CH:14]=[C:15]([CH:21]=[CH:22][CH:23]=1)[C:16]([O:18][CH2:19][CH3:20])=[O:17].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH2:19]([O:18][C:16](=[O:17])[C:15]1[CH:21]=[CH:22][CH:23]=[C:13]([O:12][C:2]2[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=2[N+:9]([O-:11])=[O:10])[CH:14]=1)[CH3:20]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 85 °C
Procedure
2,5-Difluoronitrobenzene (5.0 g, 31.4 mmol), ethyl 3-hydroxybenzoate (5.2 g, 31.4 mmol), and K2CO3 (8.7 g, 62.8 mmol) were added to DMF (50 mL). The solution was heated to 85° C. and stirred for 16 h. The reaction was cooled. The reaction was poured into distilled water and extracted with ethyl acetate. The combined organic layers were washed with distilled water, brine, and dried over sodium sulfate, filtered and concentrated under vacuum giving the crude title compound. The crude product was purified by silica gel column chromatography eluting with hexanes/ethyl acetate (90:10) to give the title compound (7.0 g, 73%).
Workup
- temperatureThe reaction was cooled
- additionThe reaction was poured
- distillationinto distilled water
- extractionextracted with ethyl acetate
- washThe combined organic layers were washed with distilled water, brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under vacuum
- customgiving the crude title compound
- customThe crude product was purified by silica gel column chromatography
- washeluting with hexanes/ethyl acetate (90:10)
Sources & evidence
- ORD record
- ord-b0338ab181f842309a46497eb57dbfb3
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07763731B2
Reaction notes
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