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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552446Generated: October 31, 2026

Water → 4-bromo-2-propyl-3-[(tetrahydro-2H-pyran-2-yloxy)methyl]phenol

https://huagongshe.com/reaction/552446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,4-dihydro-2H-pyranHCID 8080—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant4-Bromo-3-(hydroxymethyl)-2-propylphenolHCID 57900828—
SolventDichloromethaneHCID 6344—
Product4-bromo-2-propyl-3-[(tetrahydro-2H-pyran-2-yloxy)methyl]phenolHCID 5790078970%

Reaction Steps

To a solution of 4-bromo-3-(hydroxymethyl)-2-propylphenol (1.04 g, 4.24 mmol) in dichloromethane (50 mL), p-toluenesulfonic acid-hydrate (81 mg, 0.424 mmol) and 3,4-dihydro-2H-pyrane (535 mg, 6.36 mmol) were added at room temperature. The mixture was stirred at same temperature for 5 hours. The reaction solution was added with water and extracted with chloroform. Subsequently, the organic layer was washed with saturated saline, dried using anhydrous sodium sulfate, and concentrated in vacuum. The residue was purified by silica-gel column chromatography (hexane/ethyl acetate) and the title compound (972 mg, 70%) was obtained as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951822B2
Source datasetuspto-grants-2011_05
ORD IDord-d0b79bdfb69d4727acf3ad2ad6ab353e
Source noteuspto-grants-2011_05