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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
ReactantBenzophenone imineHCID 136809—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 15545158HCID 1554515876.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323366B1
Source datasetuspto-grants-2001_11
ORD IDord-5ccb35298d7d40fa9ba15f23b0c5a50e
Source noteuspto-grants-2001_11