HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128543Generated: October 26, 2026
Potassium Carbonate → 2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzene
https://huagongshe.com/reaction/128543
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenol, 2-chloro-4-fluoro-5-nitro- | HCID 158655 | — |
| Reactant | Cyclopentyl 4-methylbenzene-1-sulfonate | HCID 317685 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Fluoro-4-chloro-5-cyclopentyloxynitrobenzene | HCID 19374470 | 92.6% |
Reaction Steps
A solution of 2-fluoro-4-chloro-5-hydroxynitrobenzene (7.1 g, 37.1 mmol) and potassium carbonate (5.1 g, 37.1 mmol) in acetonitrile (300 ml) was stirred for 2 hours at a refluxing temperature. Cyclopentyl p-toluenesulfonate (10.3 g, 40.8 mmol) was added thereto, followed by stirring further for 2 hours under refluxing. After completion of the reaction, the solvent was distilled off under reduced pressure from the reaction mixture, 1N hydrochloric acid (800 ml) was added thereto, and the mixture was extracted with ethyl acetate (100 ml×3 times). The organic layer was washed with an aqueous solution of sodium bicarbonate and water, dried, and the solvent was distilled off under reduced pressure to obtain 2-fluoro-4-chloro-5-cyclopentyloxynitrobenzene as a yellow solid (8.93 g, 34.3 mmol, 92.6% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05464811 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-e6cee3e6b5ac4c1d9fc5123fc3052065 |
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| Source note | uspto-grants-1995_11 |
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