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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 3'-Chloro-6-fluoro-2-methoxy-biphenyl | HCID 58020313 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | (3'-Chloro-2-fluoro-6-methoxy-biphenyl-3-yl)-(4-nitro-phenyl)-methanone | HCID 58019914 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791267B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-fa1ba33d9765411ba0d66157ae3a9f2d |
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| Source note | uspto-grants-2014_07 |
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