Acetic Acid → HCID 22343609, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[CH:5]=[C:4]([F:11])[C:3]=1[F:12].C(O)(=O)C>[Fe].CO>[Cl:1][C:2]1[CH:7]=[C:6]([CH:5]=[C:4]([F:11])[C:3]=1[F:12])[NH2:8]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 62.5 °C
Procedure
1-Chloro-2,3-difluoro-5-nitrobenzene (3 g, 15.6 mmol) was added to acetic acid (10 mL) and methanol (250 mL). To this mixture was added iron powder (3.0 g) in portions, stirred for 2 h at 60-65° C., cooled to room temperature, and filtered. The filterate was stripped to a brown solid, which was extracted with ethyl acetate (3×200 mL), washed with 1N NaOH (3×100 mL), and brine (2×100 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered and stripped down to yield the product as a pale yellow solid (2.6 g). Yield 100%; 1H NMR (400 MHz, CDCl3): δ 6.41 (m, 2 H), 3.65 (br s, 2 H) ppm.
Workup
- temperaturecooled to room temperature
- filtrationfiltered
- extractionwas extracted with ethyl acetate (3×200 mL)
- washwashed with 1N NaOH (3×100 mL), and brine (2×100 mL)
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- filtrationfiltered
Sources & evidence
- ORD record
- ord-43f4872f14134396b275fd84996cd3bf
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08853186B2
Reaction notes
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