HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 66742678, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (2-Bromo-1,3-thiazol-5-yl)methanol | HCID 7213124 | — |
| Reactant | HCID 57591516 | HCID 57591516 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66742678 | HCID 66742678 | 81.9% |
Reaction Steps
To a solution of (2-bromothiazol-5-yl)methanol (4.85 g, 25 mmol) and 4-chloro-bicyclo[3.2.1]oct-3-en-2-one (3.92 g, 25 mmol) in anhydrous tetrahydrofuran (100 ml) is added, in small portions, sodium hydride (60% dispersion in oil, 1.00 g, 25 mmol) at 0° C. The reaction mixture is stirred overnight and allowed to warm to room temperature. Silica gel is added to the crude reaction mixture, the solvent is evaporated under reduced pressure and the residue is purified by flash chromatography on silica gel to give 4-(2-bromothiazol-5-ylmethoxy)bicyclo[3.2.1]oct-3-en-2-one (6.43 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541594B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-969395d855b04c7fbb15e86f4ffde491 |
| Source note | uspto-grants-2013_09 |