Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636937Generated: November 1, 2026

Water → 4-[(4-Bromophenyl)methoxy]tetrahydro-2H-pyran

https://huagongshe.com/reaction/636937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromobenzyl bromideHCID 68527—
ReactantTetrahydro-4H-pyran-4-olHCID 74956—
SolventDimethylformamideHCID 6228—
Product4-[(4-Bromophenyl)methoxy]tetrahydro-2H-pyranHCID 22665681—

Reaction Steps

A mixture of 2.90 mL of 4-hydroxy-tetrahydropyran in 30 mL of dry N,N-dimethylformamide was added dropwise to a stirred suspension of 0.84 g of sodium hydride (95%, dispersion in mineral oil) in 30 mL of dry N,N-dimethylformamide at 5° C. The resulting clear solution was allowed to come to room temperature and stirring was continued for 24 hours, followed by dropwise addition of 9.40 g of 4-bromo-benzylbromide in 50 mL of dry N,N-dimethylformamide at 5° C. and stirring at room temperature for 24 hours. The mixture was poured into water and extracted with ethyl acetate. The combined extracts were washed with water and brine, dried (sodium sulfate), and concentrated. The residue was purified by silica chromatography (isohexane/ethyl acetate=9/1, 8/2, 7/3, 6/4 v/v) yielding 5.40 g of 4-(4-bromo-benzyloxy)-tetrahydropyran as an oil. EI-MS: 270 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194409B1
Source datasetuspto-grants-2001_02
ORD IDord-9a472db8b5fe4c93978e05845eb0d63d
Source noteuspto-grants-2001_02