HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → (2-Ethyl-1,3-thiazol-5-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 21408257 | HCID 21408257 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Ethyl-1,3-thiazol-5-yl)methanol | HCID 21408258 | 94.2% |
Reaction Steps
2.4 g of mixed lithium aluminum hydride was added under nitrogen to a solution of 11.3 g of methyl 2-ethyl-thiazole-5-carboxylate in 100 ml of anhydrous tetrahydrofuran at 20 to 25° C and the mixture was refluxed for 1 1/2 hours. After cooling the mixture, excess lithium aluminum hydride was destroyed by the addition of ethyl acetate. The mixture was added to water and was vacuum filtered. The recovered precipitate was empasted with ethyl acetate and then with a methanol-methylene chlorine mixture. The filtrate was washed with water, dried and evaporated to dryness to obtan 9.5 g of an oil which was rectified under reduced pressure to obtain 8.9 g of 2-ethyl-thiazole-5-methanol with a boiling point of 78° C at 0.1 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04051249 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-49c31ad84948443cb38705d0e2a7dc76 |
| Source note | uspto-grants-1977_09 |