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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2-Chloro-4-fluoro-5-nitrobenzoyl chloride | HCID 15124384 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,1,2,2-Tetrachloroethane | HCID 6591 | — |
| Product | 2-Chloro-4-fluoro-5-nitrobenzophenone | HCID 18314505 | 98.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06156700 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-56719f2a02d44bf9a1671ed492afb9de |
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| Source note | uspto-grants-2000_12 |
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