HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68496Generated: October 26, 2026
Sodium Carbonate → 10-(3-Bromophenyl)benzo[c]phenanthrene
https://huagongshe.com/reaction/68496
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-Bromo-4-iodobenzene | HCID 11522 | — |
| Reactant | Phenanthren-2-ylboronic acid | HCID 46835781 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 10-(3-Bromophenyl)benzo[c]phenanthrene | HCID 86649136 | 158.1% |
Reaction Steps
Under an argon atmosphere, 22.2 g of phenanthrene-2-boronic acid, 28.3 g of 4-bromoiodobenzene, 2.31 g of tetrakis(triphenyl phosphine) palladium(0), 400 mL of toluene, and 200 mL of a 2-M aqueous solution of sodium carbonate were loaded, and then the mixture was stirred for 8 hours under reflux. After having been cooled to room temperature, the reaction solution was extracted with toluene. The water layer was removed, and the organic layer was sequentially washed with water and a saturated salt solution, and was then dried with magnesium sulfate. After magnesium sulfate had been separated by filtration, the organic layer was concentrated. The residue was purified by silica gel column chromatography. Thus, 30.3 g of 10-(3-bromophenyl)benzo[c]phenanthrene were obtained (91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822041B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-071fb915539e455fb8e11aa1d9dc2550 |
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| Source note | uspto-grants-2014_09 |
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