Ethanol → HCID 16775461, compound

HRID 2186951Notes

Reaction equation

HRID 2186951 reaction equation
[F:1][C:2]1[CH:20]=[CH:19][CH:18]=[CH:17][C:3]=1[C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-])=O)=[CH:9][C:8]=1[CH3:16])=[O:5].C1CCCCC=1.C(O)C>[Pd].O>[NH2:13][C:10]1[CH:11]=[CH:12][C:7]([NH:6][C:4](=[O:5])[C:3]2[CH:17]=[CH:18][CH:19]=[CH:20][C:2]=2[F:1])=[C:8]([CH3:16])[CH:9]=1

Participants

6

Reactant 3

HCID 702EthanolHCID 8079CyclohexeneHCID 40507012-Fluoro-N-(2-methyl-4-nitrophenyl)benzamide

Product 1

HCID 16775461HCID 16775461, compound

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 962WaterSolvent

Conditions

Temperature
4 °C

Procedure

A mixture of 2-fluoro-N-(2-methyl-4-nitrophenyl)benzamide (4.55 g), cyclohexene (30 mL), ethanol (70 mL), water (30 mL) and 10% palladium on charcoal (3 g) is heated at reflux for 30 minutes. The mixture is filtered through diatomaceous earth and concentrated under reduced pressure. The resulting oil is dissolved in 50 niL of ethyl acetate and cooled at 4° C. for 12 hours. Filtration provides the product as a tan solid.

Workup

  1. temperatureis heated
  2. temperatureat reflux for 30 minutes
  3. filtrationThe mixture is filtered through diatomaceous earth
  4. concentrationconcentrated under reduced pressure
  5. dissolutionThe resulting oil is dissolved in 50 niL of ethyl acetate
  6. filtrationFiltration

Sources & evidence

ORD record
ord-32c9b879465648bb9ddcd7ad27d39838
Source dataset
uspto-grants-2002_06
Patent number
US06407123B1

Reaction notes

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