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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517112Generated: October 30, 2026

2-Bromoethanol → 2-(3-BroMo-phenoxy)-ethanol

https://huagongshe.com/reaction/517112

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromophenolHCID 11563—
SolventAcetoneHCID 180—
Product2-(3-BroMo-phenoxy)-ethanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115056B2
Source datasetuspto-grants-2015_08
ORD IDord-37f2d13c4f3a48d78c6c5725a9b2a89d
Source noteuspto-grants-2015_08