HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086821Generated: October 28, 2026
Bromocyclopentane → 1-Cyclopentyloxy-2-methoxy-5-nitrobenzene
https://huagongshe.com/reaction/2086821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methoxy-5-nitrophenol | HCID 69471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Cyclopentyloxy-2-methoxy-5-nitrobenzene | HCID 11390741 | — |
Reaction Steps
A mixture of 2-methoxy-5-nitrophenol (4.86 g), cyclopentyl bromide (3.4 ml) and potassium carbonate (4.8 g) in N,N-dimethylformamide (50 ml) was stirred at 50° C. for 3 hours. Then the mixture was poured into a mixture of ethyl acetate and aqueous sodium bicarbonate. The organic phase was separated, washed with aqueous sodium bicarbonate and brine, dried over magnesium sulfate and concentrated. The resultant solid was collected and washed with isopropyl ether to give 3-cyclopentyloxy-4-methoxy-1-nitrobenzene (5.05 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06727245B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-b3d20bea732745098e81d4a5fbe5d90a |
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| Source note | uspto-grants-2004_04 |
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