Acetyl chloride → HCID 53660605, compound

HRID 1460192Notes

Reaction equation

HRID 1460192 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

6

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

  1. temperatureThe solution was then chilled with ice
  2. stirringThe mixture was well shaken
  3. 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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