HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → N-triphenylmethyl-2-methylaminocarbonylthioethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | N-triphenylmethylcysteamine | HCID 15616512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-triphenylmethyl-2-methylaminocarbonylthioethylamine | HCID 15616514 | 79% |
Reaction Steps
Methylisocyanate (243 mg) was dissolved in anhydrous dichloromethane (5 ml). To the solution were added N-triphenylmethylcysteamine (3.19 g: 0.33 equimolar amount) while cooling with ice. The reaction solution was stirred at room temperature for 4 hours and was concentrated under reduced pressure. The residue was dissolved in chloroform (50 ml), and the chloroform solution was well washed with water and a saturated solution of sodium chloride. Anhydrous sodium sulate was used to dry the chloroform layer which was then concentrated under reduced pressure. The residue was purified by silica gel chromatography using a solvent system of hexane/ethyl acetate (5:1 v/v) to obtain the desired substance (297 mg) with a yield of 79%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863935 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-88a1850dfd1e43d28f014436e301362c |
| Source note | uspto-grants-1989_09 |