HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341576Generated: October 30, 2026
2-Bromoethanol → 2-(3-BroMo-phenoxy)-ethanol
https://huagongshe.com/reaction/341576
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromophenol | HCID 11563 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(3-BroMo-phenoxy)-ethanol | HCID 10536727 | — |
Reaction Steps
To a solution of 3-bromophenol (14) (36.38 g, 210.3 mmol) in acetone (175 ml) was added K2CO3 (0.033 g, 237 mmol) and 2-bromoethanol (20 ml, 283.3 mmol). The mixture was heated to reflux for 4 d under argon then cooled to room temperature. The solids were removed by filtration and the filtrate concentrated under reduced pressure. The residue was dissolved in diethyl ether (150 ml) and washed with water (100 ml), aqueous NaOH (10%, 100 ml, 3×50 mL, 5%, 200 ml), water (100 ml), and brine, dried over MgSO4 and concentrated under reduced pressure to give 2-(3-bromophenoxy)ethanol (15) as light brown oil. Yield (21.07 g, 46%): 1H NMR (400 MHz, CDCl3) δ 7.14 (t, J=7.8 Hz, 1H), 7.07-7.12 (m, 2H), 6.85 (ddd, J=7.8, 2.4, 1.3 Hz, 1H), 4.06 (m, 2H), 3.95 (m, 2H), 2.11 (t, J=12.3 Hz. 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895782B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-1e4f46aef5584219831905d71b1c3c47 |
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| Source note | uspto-grants-2014_11 |
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