Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632066Generated: October 30, 2026

4-Nitrobenzoyl chloride → (3'-Chloro-2-fluoro-6-methoxy-biphenyl-3-yl)-(4-nitro-phenyl)-methanone

https://huagongshe.com/reaction/1632066

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3'-Chloro-6-fluoro-2-methoxy-biphenylHCID 58020313—
SolventNitrobenzeneHCID 7416—
Product(3'-Chloro-2-fluoro-6-methoxy-biphenyl-3-yl)-(4-nitro-phenyl)-methanoneHCID 5801991491%

Reaction Steps

To a solution of 4-nitro-benzoyl chloride (1900 mg, 10.2 mmol) in nitrobenzene (6 mL) was added aluminum trichloride (1360 mg, 10.2 mmol) at 0° C. The mixture was allowed to warm to room temperature and stirred at room temperature for 1 h, cooled to 0° C., and 3′-chloro-6-fluoro-2-methoxy-biphenyl (2.01 g, 8.5 mmol) in nitrobenzene (1 mL) was added at 0° C. The reaction mixture was allowed to warm to room temperature and stirred 24 h. The reaction mixture was cooled to −10° C. and quenched with ice-water (50 mL), extracted with ethyl acetate (2×25 mL), washed with water (2×10 mL), saturated aqueuos sodium bicarbonate (10 mL), brine (30 mL), and dried over Na2SO4. After filtration and removal of solvent, the crude was purified by crystallization from ether-hexane to give I-133 (3.00 g, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791267B2
Source datasetuspto-grants-2014_07
ORD IDord-fa1ba33d9765411ba0d66157ae3a9f2d
Source noteuspto-grants-2014_07