HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium ethoxide → (2-((Dimethylamino)methyl)thiazol-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 4-Thiazolol, 4-(chloromethyl)-2-[(dimethylamino)methyl]-4,5-dihydro- | HCID 10330702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2-((Dimethylamino)methyl)thiazol-4-yl)methanol | HCID 1838020 | — |
Reaction Steps
To a 100 ml, three necked, flask equipped with an agitator and a condensor were added 3.0 g (0.014 mol) of 2-hydroxy-2-chloromethyl-2-(dimethylaminomethyl)thiazoline (prepared as in Example 1), 50 ml of toluene and 0.95 g (0.014 mol) of sodium ethoxide. The resulting solution was stirred at room temperature for 30 minutes. A 1 ml sample of the reaction mixture was then removed from the flask and diluted according to the procedure described in Example 4. The HPLC assay set forth in Example 3 indicated that 6.6% of the thiazoline substrate had converted to the desired titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05457206 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-1c642810d75447799f4c1853b1054561 |
| Source note | uspto-grants-1995_10 |