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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449110Generated: October 30, 2026

Benzene → HCID 21618736, compound

https://huagongshe.com/reaction/449110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantHydrochloric AcidHCID 313—
ReactantThionyl ChlorideHCID 24386—
Reactant4-Bromo-2-fluorobenzoic acidHCID 302681—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDimethylformamideHCID 6228—
ProductHCID 21618736HCID 21618736—

Reaction Steps

In an oven dried flask was added 2-fluoro-4-bromobenzoic acid (1.00 g, 4.25 mmol), thionyl chloride (0.77 mL, 0.010 mol) and a drop of DMF and the reaction was refluxed for 2 h. The excess thionyl chloride was then distilled off and the residual thionyl chloride was removed on the pump. Benzene (20 mL, 0.2 mol) and aluminum trichloride (0.676 g, 5.07 mmol) were added to the reaction mixture. The reaction mixture was stirred at room temp for 1 h. The crude reaction mixture was poured onto ice and conc. HCl (15 mL). The organic layer was separated and the aqueous layer extracted with EtOAc. The combined organic phases were washed with 5% aq NaOH solution, water and dried (Na2SO4). The organic phase was concentrated in vacuo to give a residue which was purified by silica gel chromatography, eluting with 2% EtOAc in hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481733B2
Source datasetuspto-grants-2013_07
ORD IDord-3575b92d91324465a99012c0d86aac21
Source noteuspto-grants-2013_07