HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 10-{[(Methylsulfanyl)carbonothioyl]amino}decane-1-sulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 10354160 | HCID 10354160 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 10-{[(Methylsulfanyl)carbonothioyl]amino}decane-1-sulfonic acid | HCID 21315098 | — |
Reaction Steps
A suspension of 56 g. (1.0 mol.) of potassium hydroxide and 118.7 g. (0.5 mol.) of 10-aminodecanesulfonic acid in 170 ml. of water is stirred for 30 minutes at 25°, then 40 g. (0.52 mol.) of carbon disulfide and 80 ml. of ethanol are added and the reaction mixture is stirred at 25° for 12 hours. The mixture is refluxed gently for 2 hours and cooled. Methyl iodide (71 g., 0.3 mol.) and 130 ml. of ethanol are added to the mixture and it is stirred at 25° for 12 hours. The mixture is evaporated to remove the ethanol and the solid residue is collected by filtration to give methyl 10-sulfodecyldithiocarbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04093723 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-41fa4d4c5c6744518c05127bba3c8ed5 |
| Source note | uspto-grants-1978_06 |