HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178671Generated: October 29, 2026
2-Bromophenol → 1-bromo-2-(2-bromoethoxy)benzene
https://huagongshe.com/reaction/2178671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-bromo-2-(2-bromoethoxy)benzene | HCID 2734928 | — |
Reaction Steps
A suspension of 2-bromophenol (3.50 g, 20.23 mmol), 1,2-dibromoethane (19.00 g, 101 mmol), and potassium carbonate (7.06 g, 2.92 mmol) in acetonitrile (50 mL) was heated to 80° C. After heating overnight, the reaction mixture was cooled to room temperature, diluted with ethyl acetate and washed with water and saturated aqueous sodium chloride solution. The organic layer was dried over magnesium sulfate, filtered and the filtrate was concentrated in vacuo to afford the title compound as a clear oil. Yield: 6.36 g, 100%. 1H NMR (400 MHz, CDCl3) δ 3.69 (dd, J=6.6, 6.4 Hz, 2H), 4.35 (dd, J=6.7, 6.4 Hz, 2H), 6.87-6.94 (m, 2H), 7.25-7.30 (m, 1H), 7.56 (dd, J=7.9, 1.6 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067934B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-1e2ee62ebde04d58ab5b06f5a8e34e97 |
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| Source note | uspto-grants-2015_06 |
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