Sodium Acetate → HCID 73753155, compound
Reaction equation
[C:1]([C:4]1[CH:19]=[CH:18][C:7]([O:8][CH2:9][C:10]2[CH:17]=[CH:16][C:13]([CH:14]=O)=[CH:12][CH:11]=2)=[C:6]([CH2:20][CH2:21][CH3:22])[C:5]=1[O:23][C:24](=[O:26])[CH3:25])(=[O:3])[CH3:2].C([O-])(=O)C.[Na+].[S:32]1[CH2:38][C:36](=[O:37])[NH:35][C:33]1=[S:34]>C(O)(=O)C>[C:1]([C:4]1[CH:19]=[CH:18][C:7]([O:8][CH2:9][C:10]2[CH:17]=[CH:16][C:13]([CH:14]=[C:38]3[S:32][C:33](=[S:34])[NH:35][C:36]3=[O:37])=[CH:12][CH:11]=2)=[C:6]([CH2:20][CH2:21][CH3:22])[C:5]=1[O:23][C:24](=[O:26])[CH3:25])(=[O:3])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Under a nitrogen atmosphere in a round bottom flask 4-[(4-acetyl-3-acetoxy-2-propylphenoxy)methyl]benzaldehyde (70 mg, 0.20 mmol) was dissolved in acetic acid (1 ml). To this solution was added sodium acetate (59 mg, 0.72 mmol) and then rhodanine (27.5 mg, 0.21 mmol). The reaction mixture was then heated to reflux and the progress of the reaction was monitored by thin layer chromatography.
Workup
- temperatureThe reaction mixture was then heated
- temperatureto reflux
Sources & evidence
- ORD record
- ord-9a7e73403d0644aa872edad0f66445e7
- Source dataset
- uspto-grants-1998_05
- Patent number
- US05747517
Reaction notes
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