HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 11-{[(Methylsulfanyl)carbonothioyl]amino}undecanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 11-Aminoundecanoic acid | HCID 17083 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 11-{[(Methylsulfanyl)carbonothioyl]amino}undecanoic acid | HCID 20574078 | — |
Reaction Steps
A suspension of 56 g. (1.0 mol.) of potassium hydroxide and 100 g. (0.5 mol.) of 11-aminoundecanoic acid in 170 ml. of water was stirred for 30 minutes at 25° then 40 g. (0.52 mol.) of carbon disulfide and 80 ml. of ethanol were added and the reaction mixture was stirred at 25° for 12 hours. The mixture was refluxed gently for two hours and cooled. Methyl iodide (71 g., 0.3 mol.) and 130 ml. of ethanol were added to the mixture and it was stirred at 25° for 12 hours. The mixture was evaporated to remove the ethanol and the solid residue was collected by filtration to give methyl 10-carboxydecyldithiocarbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04220644 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-793b1a78e0fc48e9953bc342bff6b68e |
| Source note | uspto-grants-1980_09 |