HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 5-(4-Ethyl-thiophen-2-ylmethoxy)-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Ethyl-2-thiophenemethanol | HCID 23261287 | — |
| Reactant | 5-Chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one | HCID 68567844 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(4-Ethyl-thiophen-2-ylmethoxy)-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one | HCID 68570023 | 88.7% |
Reaction Steps
To a solution of (4-ethyl-thiophen-2-yl)methanol (369 mg, 2 mmol) in THF (10 ml) is added sodium hydride, 60% dispersion in mineral oil, (88 mg, 2.2 mmol) in one portion and the reaction stirred at room temp for 3 hours. The resulting dark yellow solution is then cooled to 0° C., and 5-Chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (341 mg, 2.4 mmol) is added and the resulting brown solution allowed to warm to ambient over 30 minutes, then stirred at room temp for 17 hours. Crude reaction is purified by flash chromatography to give 5-(4-ethyl-thiophen-2-ylmethoxy)-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one as a white solid (515 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530667B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-6690f8d29d5d4a94bbb1466d5090a09c |
| Source note | uspto-grants-2013_09 |