HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Methanesulfonate → 1-(2-Hydroxyethyl)-2-methylthioimidazoline mesylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Methanesulfonate | HCID 4156 | — |
| Reactant | 1-(2-Hydroxyethyl)-2-imidazolinethione | HCID 19785378 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 1-(2-Hydroxyethyl)-2-methylthioimidazoline mesylate | HCID 19785379 | — |
Reaction Steps
Twenty grams of 1-(2-hydroxyethyl)-2-imidazolinethione and methyl methanesulfonate (12.75 ml) are dissolved in ethyl alcohol (90 mL) and refluxed for 2 hours. The mixture is cooled to room temperature and diluted with t-butyl methyl ether (1 liter). An oil separates which solidifies on keeping the mixture in the freezer at -20° C. for a few days. The solid is then filtered, washed with butyl methyl ether and dried to give 1-(2-hydroxyethyl)-2-methylthioimidazoline mesylate, melting point 78.9°-81.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05258381 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-0ed87c03565f4cb18279d3a096d2c6be |
| Source note | uspto-grants-1993_11 |