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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835979Generated: October 30, 2026

Imidazole → 2-(4-Hydroxy-phenyl)-7-imidazol-1-ylmethyl-benzofuran-5-ol

https://huagongshe.com/reaction/1835979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantHCID 10171939HCID 10171939—
SolventDimethylformamideHCID 6228—
Product2-(4-Hydroxy-phenyl)-7-imidazol-1-ylmethyl-benzofuran-5-olHCID 1014960289.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of benzyl bromide 4 (0.070 g, 0.215 mmole) in 10 mL DMF was added imidazole (0.030 g, 0.437 mmole). After stirring at 60° C. for 3 hours, the reaction mixture was poured into water and extracted with ethyl acetate. The combined organic phases were washed with saturated sodium bicarbonate, water, brine, and dried with magnesium sulfate. The organic phases were concentrated and the residue was loaded on to silica gel and chromatographed with silica gel (hexanes:ethyl acetate, 9:1) to afford 0.059 g (88%) of imidazole 16 as a light tan solid: Mp=269-271° C.; 1H NMR (DMSO-d6) δ 9.88 (s, 1 H), 9.24 (s, 1 H), 7.88 (s, 1 H), 7.72 (d, 2 H, J=8.6 Hz), 7.26 (s, 1 H), 7.04 (s, 1 H), 6.93 (s, 1 H), 6.88 (d, 2 H, J=8.7 Hz), 6.83 (d, 1 H, J=2.3 Hz), 6.50 (d, 1 H, J=2.3 Hz), 5.46 (s, 2 H); MS 305 (M−H)−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06774248B2
Source datasetuspto-grants-2004_08
ORD IDord-9507071d6c1c433d8ccba93cf65b43d5
Source noteuspto-grants-2004_08