HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (2-((Dimethylamino)methyl)thiazol-4-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | 2-(N-Carbethoxy-N-methylamino)methyl-4-carbethoxythiazole | HCID 20402111 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-((Dimethylamino)methyl)thiazol-4-yl)methanol | HCID 1838020 | 34.8% |
Reaction Steps
To a cooled suspension of lithium aluminum hydride (8.4 g; 0.22 mole) in 80 ml of dry tetrahydrofuran was added a solution of 2-(N-carbethoxy-N-methylamino)methyl-4-carbethoxythiazole (20.0 g; 0.07 mole) [prepared in Step C] in 160 ml of dry tetrahydrofuran over a 1 hour period. The reaction mixture was heated at reflux temperature for 8 hours, then cooled and decomposed with Na2SO4 and 40% aqueous potassium hydroxide. The mixture was filtered, dried and evaporated under reduced pressure to give 4.2 g of the title compound as an oil; TLC (aluminum oxide/CH3CN) gave RF=0.45. The NMR spectrum (60 MHz) in CDCl3 gave the following resonances δ: 7.17 (s, 1H); 4.73 (d, 2H); 3.43 (s, 2H); 3.35 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04380638 |
| Source dataset | uspto-grants-1983_04 |
| ORD ID | ord-b2931723754041faa75cc8b13434c7cd |
| Source note | uspto-grants-1983_04 |