Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455021Generated: October 31, 2026

2-[2,5-Bis(benzyloxy)phenoxy]-1-phenylethanol → 2-(2-Hydroxy-2-phenylethoxy)benzene-1,4-diol

https://huagongshe.com/reaction/1455021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[2,5-Bis(benzyloxy)phenoxy]-1-phenylethanolHCID 17978469—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(2-Hydroxy-2-phenylethoxy)benzene-1,4-diolHCID 17978604—

Reaction Steps

A solution of 2-[2,5-bis(benzyloxy)phenoxy]-1-phenylethanol (3.9 g) in ethanol (175 ml) was hydrogenated in the presence of 10% palladium on charcoal (100 mg) at 30 psi. The catalyst was removed by filtration and the solvent was evaporated under reduced pressure. The residue was recrystallized from the mixture of toluene-ethyl acetate 8:1 (15 ml). The yield of 2-(2-Hydroxy-2-phenylethoxy)benzene-1,4-diol is 1.2 g. 1H NMR (DMSO-d6) δ: 3.79 (dd, J 9.6, 8.3 Hz, 1H), 4.00 (dd, J 9.6, 3.6 Hz, 1H), 4.94 (ddd, J 3.6, 8.3, 3.9 Hz, 1H), 5.66 (d, J 3.9 Hz, 1H), 6.18 (dd, J 8.5, 2.3 Hz, 1H), 6.34 (d, J 2.3, 1H), 6.57 (d, J 8.5, 1H), 7.26-7.47 (m, 5H), 7.97 (s, 1H), 8.66 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482340B2
Source datasetuspto-grants-2009_01
ORD IDord-78f143813fbb4171857fad7b5ed8bf5c
Source noteuspto-grants-2009_01