HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 87499859, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | [2-(4-Chlorophenyl)selenazol-5-yl]methanol | HCID 59562443 | — |
| Reactant | 5-Chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one | HCID 68567844 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 87499859 | HCID 87499859 | 77.8% |
Reaction Steps
To a solution of [2-(4-chlorophenyl)selenazol-5-yl]methanol (300 mg, 1.1 mmol) in dry tetrahydrofuran (5 ml) is added, in one portion, sodium hydride (60% dispersion in mineral oil, 44 mg, 1.1 mmol). The reaction mixture is stirred for 5 minutes at room temperature and 5-chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (203 mg, 1.1 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 5-[2-(4-chloro-phenyl)-selenazol-5-ylmethoxy]-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (360 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530667B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-24f0947d47314984892ce7c6d027e7fb |
| Source note | uspto-grants-2013_09 |