Hydrochloric Acid → HCID 86023720, compound
Reaction equation
[N+:1]([O-])([O-])=O.[Na+].Cl.[F:7][C:8]1[CH:9]=[C:10]([CH:12]=[CH:13][C:14]=1[F:15])[NH2:11].[C:16]([CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])#[N:17].C([O-])(=O)C.[Na+]>CCO>[C:16]([CH:18]([N:1]=[N:11][C:10]1[CH:12]=[CH:13][C:14]([F:15])=[C:8]([F:7])[CH:9]=1)[C:19]([O:21][CH2:22][CH3:23])=[O:20])#[N:17]Participants
7
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
An aqueous solution of sodium nitrate was added dropwise to an aqueous hydrochloric acid solution of 3,4-difluoroaniline under ice cooling, for stirring at the same temperature for 1.5 hours. The resulting reaction mixture was added dropwise to an aqueous EtOH solution of ethyl cyanoacetate and sodium acetate as prepared in a separate reaction flask, for stirring at ambient temperature for 2 hours, to obtain ethyl cyano[(3,4-difluorophenyl)diazenyl]acetate.
Workup
- customThe resulting reaction mixture
- customas prepared in a separate reaction flask
- stirringfor stirring at ambient temperature for 2 hours
Sources & evidence
- ORD record
- ord-abc8efc143184915bbd3625a90048413
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07879878B2
Reaction notes
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