HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromooctane → 2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,6-dibromo-4H-cyclopenta[def]phenanthrene | HCID 59431076 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthrene | HCID 12524367 | 133.6% |
Reaction Steps
2,6-dibromo-4H-cyclopenta[def]phenanthrene (2.6 g, 7.7 mmol) and octyl bromide (3.6 g, 18.5 mmol) in a 50 ml round bottom flask were dissolved with toluene (10 ml), and TBAB (tetrabutylammoniumbromide) (0.125 g, 0.385 mmol) was added thereto. A solution of NaOH (3.1 g, 77 mmol) in water (50 ml) was added to the reaction mixture, and the resultant solution was refluxed for two days. After the reaction was terminated, the reaction solution was extracted with chloroform. The organic layer was dried over MgSO4, concentrated, and purified by silica gel column chromatography (eluent: n-hexane). The eluate was distilled under a reduced pressure to remove unreacted octyl bromide, thereby giving a compound 2 (3.6 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781579B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-7cea71d735254aee958cd05afe19dc2f |
| Source note | uspto-grants-2010_08 |