HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472511Generated: October 31, 2026
Sodium Carbonate → 8,8-Dimethyl-3-(9-phenyl-9H-carbazol-3-yl)-8H-10,12b-diaza-benzo[a]aceanthrylene
https://huagongshe.com/reaction/1472511
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 3-Bromo-9-phenylcarbazole | HCID 18942624 | — |
| Reactant | 8,8-Dimethyl-8H-10,12b-diazabenzo[a]aceanthrylene-3-boronic acid | HCID 67201981 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 8,8-Dimethyl-3-(9-phenyl-9H-carbazol-3-yl)-8H-10,12b-diaza-benzo[a]aceanthrylene | HCID 70665288 | — |
Reaction Steps
36 g (110 mmol) of 8,8-dimethyl-8H-10,12b-diazabenzo[a]aceanthrylene-3-boronic acid, 35 g (110 mmol) of 3-bromo-9-phenyl-9H-carbazole and 9.7 g (92 mmol) of sodium carbonate are suspended in 350 ml of toluene, 350 ml of dioxane and 500 ml of water. 913 mg (3.0 mmol) of tri-o-tolylphosphine and 112 mg (0.5 mmol) of palladium(II) acetate are added to this suspension, and the reaction mixture is heated under reflux for 16 h. After cooling, the organic phase is separated off, filtered through silica gel, washed three times with 200 ml of water each time and subsequently evaporated to dryness. The residue is recrystallised from toluene and from CH2Cl2/isopropanol and finally sublimed in a high vacuum. Yield: 50 g (99 mmol), 89% of theory, purity according to HPLC 99.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012599B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-4a97019daae64505adfb0fb65671feea |
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| Source note | uspto-grants-2015_04 |
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