Acetyl chloride → HCID 53660605, compound
Reaction equation
[OH:1][C:2]1[C:18]([O:19][CH3:20])=[C:17]([O:21][CH3:22])[C:16]([OH:23])=[C:15]([CH3:24])[C:3]=1[CH2:4][N:5]1[CH2:10][CH2:9][N:8]([C:11]([S:13][CH3:14])=[S:12])[CH2:7][CH2:6]1.C(N([CH2:30][CH3:31])CC)C.[C:32](Cl)(=[O:34])[CH3:33].C(=O)([O-])[OH:37].[Na+]>ClCCl>[C:32]([O:1][C:2]1[C:18]([O:19][CH3:20])=[C:17]([O:21][CH3:22])[C:16]([O:23][C:30](=[O:37])[CH3:31])=[C:15]([CH3:24])[C:3]=1[CH2:4][N:5]1[CH2:10][CH2:9][N:8]([C:11]([S:13][CH3:14])=[S:12])[CH2:7][CH2:6]1)(=[O:34])[CH3:33]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
In a nitrogen atmosphere, 0.50 g (1.34 mmol.) of methyl 4-(2,5-dihydroxy-3,4-dimethoxy-6-methylbenzyl)-1-piperazinecarbodithioate was dissolved in 5 ml of dichloromethane. To the resulting solution was added 0.30 g (2.96 mmol.) of triethylamine. The solution was then chilled with ice, and to the chilled solution was dropwise added a solution of 0.25 g (2.96 mmol.) of 95%-acetyl chloride in 3 ml of dichloromethane. The mixture was then stirred for 6 hours. To the mixture were then added 10 ml of dichloromethane and a small amount of a saturated aqueous sodium hydrogen carbonate solution. The mixture was well shaken, and the organic solvent portion was taken out. The organic portion was dried over anhydrous sodium sulfate and placed under reduced pressure to give 0.63 g of methyl 4-(2,5-diacetoxy-3,4-dimethoxy-6-methylbenzyl)-1-piperazinecarbodithioate as an oil.
Workup
- temperatureThe solution was then chilled with ice
- stirringThe mixture was well shaken
- dry with materialThe organic portion was dried over anhydrous sodium sulfate
Sources & evidence
- ORD record
- ord-99b15ded81b14cf89ee4798cd617fad4
- Source dataset
- uspto-grants-1991_12
- Patent number
- US05070089
Reaction notes
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