3-Aminobenzonitrile → HCID 21938063, compound
Reaction equation
F[C:2]1[CH:3]=[C:4]([O:11][CH3:12])[CH:5]=[CH:6][C:7]=1[N+:8]([O-:10])=[O:9].[NH2:13][C:14]1[CH:15]=[C:16]([CH:19]=[CH:20][CH:21]=1)[C:17]#[N:18]>C(OCC)(=O)C>[CH3:12][O:11][C:4]1[CH:5]=[CH:6][C:7]([N+:8]([O-:10])=[O:9])=[C:2]([NH:13][C:14]2[CH:15]=[C:16]([CH:19]=[CH:20][CH:21]=2)[C:17]#[N:18])[CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2 g of 3-fluoro-4-nitroanisole and 15 ml of 3-aminobenzonitrile were stirred for 65 hours at 140° C. The batch was then diluted with ethyl acetate, washed three times with water and once with saturated sodium chloride solution, dried on sodium sulfate, concentrated by evaporation in a vacuum, and the residue was chromatographed on silica gel.
Workup
- washwashed three times with water
- dry with materialonce with saturated sodium chloride solution, dried on sodium sulfate
- concentrationconcentrated by evaporation in a vacuum
- customthe residue was chromatographed on silica gel
Sources & evidence
- ORD record
- ord-afa39d42dc2b4ee682928e6589f2e700
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07345075B2
Reaction notes
Loading…