HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402782Generated: October 25, 2026
Water → 4-Bromo-1-[(3-methylbut-3-en-1-yl)oxy]-2-(propan-2-yl)benzene
https://huagongshe.com/reaction/402782
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2-methylbut-1-ene | HCID 549585 | — |
| Reactant | 4-Bromo-2-(propan-2-yl)phenol | HCID 14793482 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-1-[(3-methylbut-3-en-1-yl)oxy]-2-(propan-2-yl)benzene | HCID 68092937 | — |
Reaction Steps
4-Bromo-2-isopropylphenol (897 mg, 4.17 mmol) was dissolved in DMF (4.17 mL) and 4-bromo-2-methylbut-1-ene (1.24 g, 8.34 mmol) was added followed by K2CO3 (1.15 g, 8.34 mmol). The reaction mixture was heated to 60° C. overnight, cooled to room temperature, and diluted with Hexanes:EtOAc (1:1). Water was added and the organic layer was separated, dried over Na2SO4, filtered, and concentrated under vacuum. The crude residue was purified by silica gel chromatography, eluting with 0-15% EtOAc/Hexanes to give the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742110B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-b499425db2e342b09c0e0d781b637b37 |
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| Source note | uspto-grants-2014_06 |
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