HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684319Generated: November 3, 2026
Water → 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine
https://huagongshe.com/reaction/1684319
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bis(2-chloro-4-fluoro-5-aminophenyl)carbonate | HCID 15766649 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-5-(cyclopentyloxy)-2-fluorobenzenamine | HCID 15279389 | 192.7% |
Reaction Steps
A round-bottomed flask (50 cc) was charged with bis(5-amino-2-chloro-4-fluorophenyl)carbonate (1.52 g, 4.36 mmol), cyclopentyl bromide (1.39 g, 9.29 mmol) and tetrabutylammonium bromide (74 mg, 0.23 mmol) to prepare a solution in toluene (12 mL). Subsequently, 48% sodium hydroxide in aqueous solution (6 mL) was added slowly and the mixture was stirred under heating at 80° C. for 1 h. After completion of the reaction, the reaction mixture was cooled to room temperature and water (15 mL) was added, followed by extraction with toluene (10 mL×2). The organic layers were combined and washed with water (10 mL×2). The solvent was distilled off under vacuum from the resulting toluene solution, thereby giving 4-chloro-5-cyclopentyloxy-2-fluoroaniline (1.93 g, 8.40 mmol; yield=96.3% ).
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-bfda8d0e14dd4499b2c50ac12f9c4c6e |
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| Source note | uspto-grants-1997_06 |
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