HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410295Generated: November 2, 2026
Allyl bromide → 1-(Allyloxy)-2-bromo-5-chloro-4-(4-ethoxybenzyl)benzene
https://huagongshe.com/reaction/1410295
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-chloro-4-(4-ethoxybenzyl)phenol | HCID 71117194 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(Allyloxy)-2-bromo-5-chloro-4-(4-ethoxybenzyl)benzene | HCID 86728582 | 95% |
Reaction Steps
To a solution of 2-Bromo-5-chloro-4-(4-ethoxybenzyl)phenol (7, 55 mmol) in acetone (180 mL) were added potassium carbonate (15.2 g, 110 mmol) and allyl bromide (7 mL, 83 mmol) and heated at 65° C. for 3 h. The insoluble material was removed by filter and the filtrate was evaporated under reduced pressure. The crude residue was purified on Biotage® purification apparatus (silica gel, 3 to 10% ethyl acetate in hexanes) to yield the title compound (21 g, 52 mmol, 95%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921412B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-92f298d08a9e4a669cd2a312da931b70 |
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| Source note | uspto-grants-2014_12 |
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