Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | (1,1'-Biphenyl)-2-ol | HCID 7017 | — |
| Reactant | 3'-Methoxy[1,1'-biphenyl]-2-ol | HCID 12465086 | — |
| Reactant | HCID 22616539 | HCID 22616539 | — |
| Reactant | HCID 86714195 | HCID 86714195 | — |
| Product | 4-Methoxydibenzofuran | HCID 11994197 | — |
Reaction Steps
The reaction was conducted according to the General Procedure by heating 4-MeO-dibenzofuran (8, 89 mg, 0.5 mmol, 1 equiv.), KOt-Bu (112 mg, 1 mmol, 2 equiv.) and Et3SiH (401 microliters, 2.5 mmol, 5 equiv.) in 2 ml of toluene for 20 hours at 100° C. After aqueous work up, the crude reaction mixture was purified by chromatography on silica using hexanes and hexanes-ether to recover unconsumed starting material 8 (3 mg, 0.015 mmol, 3%) and isolate dibenzofuran (1, 8.4 mg, 0.05 mmol, 10%; since fractions of 1 contained small amounts of starting 8, quantification was done by 1H-NMR with CH2Br2 as an internal standard), 1,1′-biphenyl-2-ol (2, 4.3 mg, 0.025 mmol, 5%), 4-Et3Si-dibenzofuran (3, 11 mg, 0.039 mmol, 8%), 2-methoxy-6-phenyl-phenol (9, mg, 0.025 mmol, 5%), 2-(3′-methoxyphenyl)phenol (10, 47 mg, 0.235 mmol, 47%). Note: only compounds with the yield exceeding 2% were characterized. 1H and 13C NMR spectral assignments of 9 and 10 were consistent with literature reports.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309269B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-251217a8ed304915a95b3475f9159fd3 |
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| Source note | uspto-grants-2016_04 |
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