HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049923Generated: October 31, 2026
Bromocyclopentane → 1-bromo-3-(cyclopentyloxy)benzene
https://huagongshe.com/reaction/1049923
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromophenol | HCID 11563 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-bromo-3-(cyclopentyloxy)benzene | HCID 18980480 | 75% |
Reaction Steps
A mixture of 3-bromophenol (commercially available) (1.72 g, 10 mmol), bromocyclopentane (commercially available) (2.96 g, 20 mmol), and K2CO3 (2.56 g, 20 mmol) in acetone (30 mL) was stirred at 80° C. for 18 h. The solvent was removed under reduced pressure and the mixture was extracted with EtOAc (100 mL×2). The combined organic layers was washed with sat NaCl (50 mL), dried over Na2SO4, concentrated, and purified by column to give the title product (1.8 g, yield 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382241B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-8a8e81951f3b47faabc830d85e177b3f |
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| Source note | uspto-grants-2016_07 |
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