Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dibromophenol | HCID 11847 | — |
| Reactant | 3,3-Dimethyl-1-butyne | HCID 13512 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59598461 | HCID 59598461 | 26% |
Reaction Steps
3,3-Dimethylbut-1-yne (1.6 g, 20 mmol) was added to a solution of 2,6-dibromophenol (5.0 g, 20 mmol) and Cu2O (1.7 g, 12 mmol) in dry pyridine (50 mL) under N2, then the mixture was heated to about 55° C. and stirred overnight. The mixture was filtered and the filtrate was concentrated to give a residue, which was dissolved in EtOAc. This solution was washed with brine and dried over Na2SO4. The solvent was removed and the residue was purified by column chromatography to afford 7-bromo-2-tert-butyl-benzofuran (1.3 g, 26%). 1H NMR (CDCl3): 1.40 (S, 9H), 6.41 (s, 1H), 7.04 (t, 1H), 7.38 (d, 1H), 7.42 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858624B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-2a0d80164c34479a93bd4f4d95d0da70 |
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| Source note | uspto-grants-2010_12 |
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