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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897511Generated: October 25, 2026

3-Phenoxybenzyl alcohol → (2-Bromo-5-phenoxyphenyl)methanol

https://huagongshe.com/reaction/897511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenoxybenzyl alcoholHCID 26295—
ReactantN-bromobutanimideHCID 67184—
SolventAcetonitrileHCID 6342—
Product(2-Bromo-5-phenoxyphenyl)methanolHCID 2234675885%

Reaction Steps

To a solution of 3-phenoxyphenyl methanol (4.0 g, 0.020 mol) in anhydrous acetonitrile was added 1-bromo-2,5-pyrrolidinedione (3.73 g, 0.021 mol) at room temperature. The mixture was stirred at room temperature for one and a half hour under an atmosphere of nitrogen. The solvents were removed under the reduced pressure. Tetrachloromethane (100 mL) was added to the residue, and the mixture was filtered. The filtrate was concentrated into the residue, and the residue was purified by flash chromatography on silica gel using ethyl acetate/n-heptane (1:5) as mobile phase to yield (2-bromo-5-phenoxyphenyl)methanol (4.7 g, 0.017 mol):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-4c6e8c4653174f90ad0e7c0236601317
Source noteuspto-grants-2005_07