HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190403Generated: October 29, 2026
Water → 3-(1-cyanocyclopropyl)-N-[4-methoxy-3-(4-nitrophenoxy)phenyl]benzamide
https://huagongshe.com/reaction/2190403
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(1-cyanocyclopropyl)-N-(3-hydroxy-4-methoxyphenyl)benzamide | HCID 67311423 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(1-cyanocyclopropyl)-N-[4-methoxy-3-(4-nitrophenoxy)phenyl]benzamide | HCID 67313663 | 89% |
Reaction Steps
To a suspension of 3-(1-cyanocyclopropyl)-N-(3-hydroxy-4-methoxyphenyl)-benzamide (1.54 mg, 5.00 mmol) and potassium carbonate (0.69 g, 5.00 mmol) in N,N-dimethylformamide (5 mL) was added 1-fluoro-4-nitrobenzene (0.78 g, 5.50 mmol), and the mixture was stirred at 60° C. for 18 hr. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane/ethyl acetate=1:1), and triturated with diethyl ether to give the title compound (1.90 g, 89%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324395B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-6d7e347e1fe3406299677c03349e9797 |
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| Source note | uspto-grants-2012_12 |
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