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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889248Generated: October 31, 2026

Benzophenone imine → 3-Bromo-2-chloro-5-fluoroaniline

https://huagongshe.com/reaction/1889248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenone imineHCID 136809—
ReactantBinap, (A+-)-HCID 634876—
Reactant1,3-Dibromo-2-chloro-5-fluorobenzeneHCID 2724604—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 86660290HCID 86660290—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product3-Bromo-2-chloro-5-fluoroanilineHCID 58553824—

Reaction Conditions

Temperature80 °C

Reaction Steps

3-bromo-2-chloro-N-(diphenylmethylene)-5-fluoroaniline. A mixture of 2,6-dibromo-4-fluoro-1-chlorobenzene (865 mg, 3 mmol), benzophenone imine (0.61 ml, 3.6 mmol), Pd2(dba)3 (137 mg, 0.15 mmol), sodium t-butoxide (432 mg, 4.5 mmol), (S)-BINAP (280 mg, 0.45 mmol), and toluene (30 ml) was heated at 80° C. for 16 h. The mixture was extracted with ethyl acetate and the combined organic phase washed with brine. The organic phase was dried over sodium sulfate and concentrated. The crude product was purified by silica gel flash chromatography (40:1 to 20:1 hexanes/ethyl acetate eluant) to provide the title compound as a powder. MS m/z 388.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501758B2
Source datasetuspto-grants-2013_08
ORD IDord-1eb46b9cc7e34f7eb2962fa592896ad9
Source noteuspto-grants-2013_08