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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274574Generated: October 31, 2026

Benzene → 2-Chloro-4-fluoro-5-nitrobenzophenone

https://huagongshe.com/reaction/1274574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantDichloromethaneHCID 6344—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Chloro-4-fluoro-5-nitrobenzoyl chlorideHCID 15124384—
SolventHydrochloric AcidHCID 313—
Solvent1,1,2,2-TetrachloroethaneHCID 6591—
Product2-Chloro-4-fluoro-5-nitrobenzophenoneHCID 1831450598.3%

Reaction Conditions

Temperature8 °C

Reaction Steps

A solution of 2-chloro-4-fluoro-5-nitrobenzoyl chloride (26.7 g, 0.112 mol) and benzene (12.0 mL, 0.134 mol) in 1,1,2,2-tetrachloroethane is cooled to 0° C. to 5° C., treated with aluminum chloride (18.1 g, 0.136 mol), stirred for 15 minutes at about 8° C., heated to and stirred at 50° C. for one hour, cooled to room temperature, and diluted sequentially with an ice-water mixture and concentrated hydrochloric acid. The organic phase is separated, washed sequentially with water and saturated sodium hydrogen carbonate solution, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a solid. Flash column chromatography of the solid using silica gel and methylene chloride gives the title product as an orange solid (30.8 g) which is identified by NMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156700
Source datasetuspto-grants-2000_12
ORD IDord-56719f2a02d44bf9a1671ed492afb9de
Source noteuspto-grants-2000_12