Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 15290081 | HCID 15290081 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15290082 | HCID 15290082 | 97.9% |
Reaction Steps
In a nitrogen atmosphere, 2.0 g of 4-(2,3,4-trimethoxybenzyl)-1-piperazinecarbodithioic acid, 0.26 g of granular sodium hydroxide, and 3 ml of methanol were mixed, and stirred atroom temperature to yield a homogeneous reaction solution. To the solution was dropwise added under chilling with ice a solution of 0.39 ml of methyliodide in 2.4 ml of methanol. After the addition was complete, the reactionsolution was stirred for 2.5 hours at room temperature. The solvent was then distilled off under reduced pressure, and chloroform and water were added to the residue. The chloroform portion was separated, washed with a saturated aqueous sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to leave 2.0 g of the desired compound as a white powder, yield 97.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05446146 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-9ee6400e693b465ebdae436e6bf57f70 |
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| Source note | uspto-grants-1995_08 |
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