Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Resorcinol | HCID 5054 | — |
| Reactant | HCID 15529893 | HCID 15529893 | — |
| Product | HCID 86623820 | HCID 86623820 | 66.4% |
Reaction Steps
121.9 g of 3-bromo-1,1′-biadamantane (349 mmol), 9.58 g of 1,3-dihydroxybenzene (87.0 mmol), 25 mL of toluene and a stirrer were charged in a 300 mL recovery flask. The mixture was heated and agitated at 130° C. for 24 hours under nitrogen flow. A solid was obtained by removing a solvent under reduced pressure. The obtained solid was purified by column chromatography, thus obtaining 37.4 g of 4,6-di[3-(1-adamantyl)-(1-adamantyl)]-1,3-dihydroxybenzene (57.8 mmol; the yield was 66.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652125B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-4d91b94eecdc453ca3f2bb418458aa9e |
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| Source note | uspto-grants-2010_01 |
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