HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → (2-((Dimethylamino)methyl)thiazol-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Thiazolol, 4-(chloromethyl)-2-[(dimethylamino)methyl]-4,5-dihydro- | HCID 10330702 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2-((Dimethylamino)methyl)thiazol-4-yl)methanol | HCID 1838020 | — |
Reaction Steps
To a 100 ml, three-necked, flask equipped with an agitator and condensor were added 3.0 g (0.014 mol) of 4-hydroxy-4-chloromethyl-2-(dimethylaminomethyl)thiazoline (prepared as in Example 1), 47 ml of toluene, 1 ml of water and 0.79 g (0.014 mol) of solid potassium hydroxide. The resulting solution was stirred at room temperature for 45 minutes. A 1 μl 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 72.6% of the thiazoline substrate had converted to the desired titled product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05334725 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-26ec6e1a572b469ba8cea2bd7a167cac |
| Source note | uspto-grants-1994_08 |