Sodium Acetate → HCID 66701954, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:33])[C:5](=[CH:9][C:10]1[C:15]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])=[CH:14][CH:13]=[CH:12][C:11]=1[O:31][CH3:32])[C:6](=O)[CH3:7])[CH3:2].Cl.[CH3:35][O:36][C:37]1[CH:42]=[CH:41][C:40]([CH2:43][S:44][C:45](=[NH:47])[NH2:46])=[CH:39][CH:38]=1.C([O-])(=O)C.[Na+]>CN(C)C=O.CCOCC>[CH2:1]([O:3][C:4]([C:5]1[CH:9]([C:10]2[C:15]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])=[CH:14][CH:13]=[CH:12][C:11]=2[O:31][CH3:32])[N:46]=[C:45]([S:44][CH2:43][C:40]2[CH:41]=[CH:42][C:37]([O:36][CH3:35])=[CH:38][CH:39]=2)[NH:47][C:6]=1[CH3:7])=[O:33])[CH3:2]Participants
6
Conditions
- Temperature
- 70 °C
Procedure
The reaction mixture containing 2-[[2-methoxy-6-pentadecyl phenyl]methylene]-3-oxobutanoic acid ethyl ester (3 g, 6.6 mmol), 2-((4-methoxyphenyl)methyl)-2-thiopseudourea hydrochloride (1.2 g, 6.6 mmol), and sodium acetate (0.6 g, 7 mmol) in dimethylformamide (30 mL) was heated at 70° C. for 4 h. The reaction was cooled to room temperature, diluted with ether, and filtered. The filtrate was washed with water, sodium bicarbonate, and brine and dried over anhydrous sodium sulfate. The solvent was evaporated, and the compound was obtained as brown viscous liquid.
Workup
- temperatureThe reaction was cooled to room temperature
- filtrationfiltered
- washThe filtrate was washed with water, sodium bicarbonate, and brine
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was evaporated
- customthe compound was obtained as brown viscous liquid
Sources & evidence
- ORD record
- ord-1a0605ce3d1342f19c1803afa3f6929e
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687511B2
Reaction notes
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