Sodium Acetate → HCID 73753155, compound

HRID 1069124Notes

Reaction equation

HRID 1069124 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

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

  1. temperatureThe reaction mixture was then heated
  2. temperatureto reflux

Sources & evidence

ORD record
ord-82f4c32a3aa84bed8aba829efb255a9c
Source dataset
uspto-grants-2001_06
Patent number
US06251928B1

Reaction notes

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