HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 66742459, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 57591516 | HCID 57591516 | — |
| Reactant | 1-[2-(4-Chlorophenyl)thiazol-5-yl]ethanol | HCID 59562475 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66742459 | HCID 66742459 | 74.9% |
Reaction Steps
To a solution of 1-[2-(4-chlorophenyl)thiazol-5-yl]ethanol (1.1 g, 4.6 mmol) in anhydrous tetrahydrofuran (20 ml) is added, in one portion, sodium hydride (60% dispersion in mineral oil, 184 mg, 4.6 mmol). The reaction mixture is stirred for 5 minutes at room temperature and 4-chlorobicyclo[3.2.1]oct-3-en-2-one (720 mg, 4.6 mmol) is added in one portion. The reaction mixture is stirred at room temperature overnight. 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-{1-[2-(4-chlorophenyl)thiazol-5-yl]ethoxy}bicyclo[3.2.1]oct-3-en-2-one (1.24 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541594B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-994e3f73ffd042758d1c8616164dfd90 |
| Source note | uspto-grants-2013_09 |