Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 86615571 | HCID 86615571 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10083945 | HCID 10083945 | — |
Reaction Steps
Under an argon gas flow, 24 g (0.083 mol) of 2,8-dimethoxychrysene and 2 L of methylene chloride were charged into a 3 L glass flask equipped with a condenser, and cooled to −60° C. Successively, 4.1 g (0.17 mol) of boron tribromide was slowly dropped into the flask, and then the contents of the flask were stirred at room temperature for 18 h. After completion of the reaction, 1 L of water was added to the flask to separate an organic layer from the reaction solution. The resultant crude crystal was short-passed through silica gel (using THF (tetrahydrofuran) as a developing solvent). The obtained product was concentrated under reduced pressure, and the resultant crude product (25 g) was directly used in the subsequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642380B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-df1e5dd85de44646b7b565f45f41de65 |
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| Source note | uspto-grants-2010_01 |
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