Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzofuran | HCID 9223 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4,5,6,7-Tetrahydro-1-benzofuran-4-one | HCID 2733541 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 19047457 | HCID 19047457 | 97% |
Reaction Steps
To a solution of 11.1 g (0.0939 mol) of benzofuran in 150 ml of ether cooled to -20° C. was added a solution of 9.39 ml (0.0939 mol) 10M n-butyllithium in hexane, and the mixture was allowed to warm to 0° C. and stirred for 30 min. The mixture was cooled to -78° C. and 10.6 g (0.078 mol) of 4,5,6,7-tetrahydrobenzofuran-4-one in 20 ml of ether was added dropwise and the mixture was allowed to warm to room temperature, and then stirred for 1 h. To the mixture was added saturated ammonium chloride solution and the resulting mixture was extracted with ethyl acetate (3×100 ml). The organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo to afford 19.3 g (97%) of 4,5,6,7-tetrahydro-4-(2-benzofuryl)benzofuran-7-ol, an oil which crystallized on standing as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05569655 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-33612ed45b1043e9bdeb75c8ce9cc4cb |
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| Source note | uspto-grants-1996_10 |
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