Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454357Generated: October 31, 2026

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

https://huagongshe.com/reaction/454357

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 numberUS08492589B2
Source datasetuspto-grants-2013_07
ORD IDord-7b62ed2b79694b9ab1fafc3c02a89ed2
Source noteuspto-grants-2013_07