HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 19388497, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19388433 | HCID 19388433 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Product | HCID 19388497 | HCID 19388497 | 50.8% |
Reaction Steps
In a nitrogen atmosphere, 1.5 g (4.6 mmol.) of 4-(3,4,5-trimethoxyphenyl)-1-piperazinecarbodithioic acid was suspended in methanol. After addition of 0.2 g of granular sodium hydroxide, the suspension was stirred at room temperature for one hour. The reaction mixture was chilled in a mixture of ice and sodium chloride. To the reaction mixture was dropwise added a solution of 0.29 ml of methyl iodide in 3.7 ml of methanol. After the addition was complete, the mixture was stirred at room temperature for 1 hour. Precipitated crystals were collected by filtration to give 0.8 g of the desired compound as a gray-brown powder, m.p. 135°-137° C. (decomp.), yield 50.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05070089 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-d7af2821433143908bc5cfcdb758903f |
| Source note | uspto-grants-1991_12 |