HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726336Generated: October 30, 2026
Pyridine → 4-fluoro-N-(4-nitrophenyl)benzamide
https://huagongshe.com/reaction/726336
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Catalyst | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-fluoro-N-(4-nitrophenyl)benzamide | HCID 3948428 | 100.2% |
Reaction Steps
To a suspension of 30.0 gm (0.217 mole) 4-nitroaniline in 225 mL dichloromethane were added 17.57 mL (0.217 mole) pyridine. The suspension was cooled to 0° C. and then 25.66 mL (0.217 mole) 4-fluorobenzoyl chloride were added slowly. Within 15 minutes the reaction mixture became homogeneous and was allowed to warm to room temperature. After an hour an additional 2.56 mL (21.7 mMol) 4-fluorobenzoyl chloride and 1.75 mL (21.7 mMol) pyridine were added and the reaction continued at room temperature for an additional hour. The reaction mixture was then washed with 200 mL water at which point a precipitate formed. The solid was filtered, washed with 100 mL hexane, washed with 200 mL water and dried under reduced pressure at 60° C. to give 56.6 gm (100%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05708187 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-04e59fadcc28436589d06bae735e3460 |
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| Source note | uspto-grants-1998_01 |
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