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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916793Generated: October 30, 2026

1-[2-(Benzyloxy)ethoxy]-4-(2-bromoethyl)benzene → 2-[4-(2-Bromoethyl)phenoxy]ethanol

https://huagongshe.com/reaction/916793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[2-(Benzyloxy)ethoxy]-4-(2-bromoethyl)benzeneHCID 68940841—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-[4-(2-Bromoethyl)phenoxy]ethanolHCID 69384360—

Reaction Steps

1-[2-(benzyloxy)ethoxy]-4-(2-bromoethyl)benzene in EtOAc (150 mL) and EtOH (50 mL) was hydrogenated over 10% Pd/C (530 mg) at room temperature and atmospheric pressure for 8 h. The catalyst was removed by filtration over Celite, washed with EtOAc and concentrated in vacuo to give the title compound (3.6 g). LCMS RT=2.82 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271197B2
Source datasetuspto-grants-2007_09
ORD IDord-dc5a031a0e4543a8a902e51c9fdb3279
Source noteuspto-grants-2007_09