HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628641Generated: October 29, 2026
2-Bromoethanol → 2-(3-BroMo-phenoxy)-ethanol
https://huagongshe.com/reaction/628641
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 (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 reaction mixture was heated at reflux under argon for 4 days. After cooling to room temperature, the mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was dissolved in diethyl ether (150 ml) and the solution was washed successively with water, 10% aqueous NaOH, 5% aqueous NaOH, water, and brine. The solution was dried over MgSO4 and concentrated under reduced pressure to give 2-(3-bromophenoxyl)ethanol (106) as a 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), 4.05-4.07 (m, 2H), 3.93-3.97 (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 | US09314467B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-ac8d963bc27b4539a9f6d7af913ca0c9 |
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| Source note | uspto-grants-2016_04 |
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