Potassium Acetate → HCID 178435581, compound
Reaction equation
[CH2:1]([C:3]1[CH:4]=[CH:5][C:6]([NH:12]/[CH:13]=[CH:14]/[N+:15]([O-:17])=[O:16])=[C:7]([CH:11]=1)[C:8](O)=[O:9])[CH3:2].C([O-])(=O)C.[K+]>C(OC(=O)C)(=O)C>[CH2:1]([C:3]1[CH:11]=[C:7]2[C:6](=[CH:5][CH:4]=1)[N:12]=[CH:13][C:14]([N+:15]([O-:17])=[O:16])=[C:8]2[OH:9])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared in analogy to Example 19b starting from 11.2 g (47.4 mmol) of 5-ethyl-2-((E)-2-nitro-vinylamino)benzoic acid (Example 49c) and 5.58 g (56.8 mmol) potassium acetate in 50 ml acetic anhydride. mp: 308-310° C. (dec.); MS: 219 (M++1); HPLC: tret=12.48 min (Grad 3).
Workup
- customtret=12.48 min (Grad 3)
Sources & evidence
- ORD record
- ord-e3d2f3238ef4412b87e7a64ae3f8180f
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07998972B2
Reaction notes
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