Sodium Acetate → HCID 73753161, compound

HRID 1069121Notes

Reaction equation

HRID 1069121 reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][O:11][C:12]2[CH:19]=[CH:18][C:15]([CH:16]=O)=[CH:14][CH:13]=2)=[C:6]([CH2:20][CH2:21][CH3:22])[C:5]=1[O:23][CH3:24])(=[O:3])[CH3:2].C([O-])(=O)C.[Na+].[S:30]1[CH2:36][C:34](=[O:35])[NH:33][C:31]1=[S:32]>C(O)(=O)C>[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][O:11][C:12]2[CH:19]=[CH:18][C:15]([CH:16]=[C:36]3[S:30][C:31](=[S:32])[NH:33][C:34]3=[O:35])=[CH:14][CH:13]=2)=[C:6]([CH2:20][CH2:21][CH3:22])[C:5]=1[O:23][CH3:24])(=[O:3])[CH3:2]

Participants

5

Procedure

Under nitrogen atmosphere in a round bottom flask 4-[(4-acetyl-3-methoxy-2-propylphenyl)methoxy]benzaldehyde (0.33 g, 1.01 mmol) was dissolved in 5 ml of acetic acid with stirring. To this solution was added sodium acetate (0.29 g, 3.53 mmol) followed by the addition of rhodanine (0.13 g, 0.98 mmol). The reaction mixture was heated to reflux. The progress of the reaction was monitored by thin layer chromatography. The reaction was allowed to reflux overnight.

Workup

  1. temperatureThe reaction mixture was heated to reflux
  2. temperatureto reflux overnight

Sources & evidence

ORD record
ord-02c410a559db4fbf921d9909b7971f67
Source dataset
uspto-grants-2001_06
Patent number
US06251928B1

Reaction notes

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