HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816685Generated: October 31, 2026
4-Bromophenol → 1-Bromo-4-((6-bromohexyl)oxy)benzene
https://huagongshe.com/reaction/1816685
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Bromo-4-((6-bromohexyl)oxy)benzene | HCID 22494750 | 80.4% |
Reaction Steps
A mixture of 4-bromophenol (10 g), 1,6-dibromohexane (49.4 g) and potassium carbonate (9.59 g) in N,N-dimethylformamide (50 ml) was stirred for 4 hours at 60° C. (bath temp.), and then cooled to ambient temperature. To the reaction mixture was added ethyl acetate (200 ml), and the mixture was washed with water (200 ml×2) and brine. The organic layer was dried over magnesium sulfate. Magnesium sulfate was filtered off, and the filtrate was evaporated under reduced pressure to give a crude product. The crude product was purified by silica gel chromatography (1:0-1:1 hexane-ethyl acetate) to give 1-bromo-4-(6-bromohexyloxy)benzene (15.61 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884868B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-20ecb62ac1ad4b3387cfedd5b1a06f08 |
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| Source note | uspto-grants-2005_04 |
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