HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430889Generated: October 30, 2026
1-Bromo-3-fluorobenzene → HCID 15545158, compound
https://huagongshe.com/reaction/430889
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-3-fluorobenzene | HCID 14082 | — |
| Reactant | Benzophenone imine | HCID 136809 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis[2-(diphenylphosphino)phenyl] ether | HCID 4285986 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15545158 | HCID 15545158 | 76.3% |
Reaction Steps
An oven-dried test tube was charged with tris(dibenzylideneacetone)dipalladium (4.6 mg, 0.005 mmol) and bis(2-(diphenylphosphino)phenyl)ether [DPE-phos] (8.2 mg, 0.015 mmol), capped with a rubber septum, evacuated and refilled with argon. Benzophenone imine (190 mg, 1.05 mmol), 3-bromofluorobenzene (175 mg, 1.0 mmol) and toluene (2 mL) were added via syringe. The resulting solution was stirred at rt for 5 minutes. The tube was opened and sodium tert-butoxide (135 mg, 1.4 mmol) was added. The tube was again capped with the septum, and additional toluene (2 mL) was added via syringe to wash the solid from the test tube wall into the solution. The solution was stirred at room temperature with a gentle argon purge for 5 minutes, then heated at 80° C. for 3 hours and 5 minutes. The reaction mixture was cooled to room temperature and washed with saturated aqueous sodium chloride (2 mL). The organic layer was filtered through celite and concentrated in vacuo. The product was isolated as a yellow solid (210 mg, 76%) by recrystalization from hot methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323366B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-5ccb35298d7d40fa9ba15f23b0c5a50e |
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| Source note | uspto-grants-2001_11 |
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