Potassium Acetate → HCID 178526770, compound
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:11]=[CH:12][CH2:13][N+:14]([O-:16])=[O:15])=[C:6]([CH:10]=1)[C:7](O)=[O:8].C([O-])(=O)C.[K+]>C(OC(=O)C)(=O)C>[F:1][C:2]1[CH:10]=[C:6]2[C:5](=[CH:4][CH:3]=1)[N:11]=[CH:12][C:13]([N+:14]([O-:16])=[O:15])=[C:7]2[OH:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4 g (17.6 mmol) of 5-fluoro-2-[2-nitro-ethylideneamino]-benzoic acid (Example 19a) in 35 ml acetic anhydride are heated (ca. 100° C.) until a clear solution is obtained. 2 g (21.2 mmol) of potassium acetate are added and stirring is continued for 30 min (tlc-control). The reaction mixture is cooled to rt and the formed crystals are filtered off and washed several times with acetic acid and water. mp: 313° C.; MS: 207 (M+−1); HPLC: tret=9.94 min (Grad 3).
Workup
- customis obtained
- filtrationthe formed crystals are filtered off
- washwashed several times with acetic acid and water
- customtret=9.94 min (Grad 3)
Sources & evidence
- ORD record
- ord-949388d34141422aa13a827ce24a5a8f
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07998972B2
Reaction notes
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