HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684312Generated: November 4, 2026
Potassium Iodide → 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine
https://huagongshe.com/reaction/1684312
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Amino-2-chloro-4-fluorophenol | HCID 158654 | — |
| Reactant | Cyclopentyl 4-methylbenzene-1-sulfonate | HCID 317685 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine | HCID 15279389 | 99.7% |
Reaction Steps
A round-bottomed flask (50 cc) equipped with a mechanical stirrer was charged with 5-amino-2-chloro-4-fluorophenol (1.02 g, 6.29 mmol), cyclopentyl p-toluenesulfonate (1.56 g, 6.50 mmol), tetrabutylammonium bromide (242 mg, 0.75 mmol) and potassium iodide (262 mg, 1.57 mmol) to prepare a solution in toluene (20 mL). Subsequently, 40% sodium hydroxide in aqueous solution (20 mL) was added slowly and the mixture was stirred under heating at 100° C. for 2 h. After completion of the reaction, the reaction mixture was cooled to room temperature and water (10 mL) was added, followed by extraction with ethyl acetate (20 mL×3). The organic layers were combined, washed with water (10 mL) and saturated brine (10 mL) and dried with anhydrous magnesium sulfate. After the desiccant was removed, the solvent was distilled off under vacuum to give 4-chloro-5-cyclopentyloxy-2-fluoroaniline (1.44 g, 6.27 mmol; yield=99.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05639915 |
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| Source dataset | uspto-grants-1997_06 |
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| ORD ID | ord-d9146d03663543cc9026f6391037306b |
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| Source note | uspto-grants-1997_06 |
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