HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-Cyclobutyl-4-thiazole methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 2-cyclobutylthiazole-4-carboxylate | HCID 54513950 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Cyclobutyl-4-thiazole methanol | HCID 53970873 | 101.1% |
Reaction Steps
Sodium borohydride (2.3 g) was added in portions over a 10 min period to an ice cold solution of 6.3 g of 2-cyclobutyl-4-thiazolecarboxylic acid ethyl ester in 100 ml of ethyl alcohol. The ice bath was removed and the reaction mixture stirred at room temperature for 30 hr during which an additional 0.46 g of sodium borohydride was added. The reaction mixture was then diluted with 200 ml of ice water and extracted with ethyl ether. The combined extracts were washed with water, dried (MgSO4) and condensed in vacuo to yield 5.1 g of 2-cyclobutyl-4-thiazole methanol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05399702 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-b6e6e4147fd74d2584f307bd85b9e15a |
| Source note | uspto-grants-1995_03 |