Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350882Generated: October 31, 2026

Diethyl Ether → 3-(Benzyloxy)-4-tert-butylphenol

https://huagongshe.com/reaction/1350882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant3-(Benzyloxy)-4-tert-butylphenyl tert-butyl carbonateHCID 21097478—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
Product3-(Benzyloxy)-4-tert-butylphenolHCID 2109747496%

Reaction Steps

To a diethylether (100 ml) solution of 3-(benzyloxy)-4-tert-butylphenyl tert-butyl carbonate (7.1 g, 20 mmol) was added lithium aluminum hydride (0.75 g, 20 mmol) at 0° C. The reaction mixture was 10 stirred at ambient temperature for 3 hours. To the mixture was added H2O (10 ml) carefully to form a white prepicitate. The organic layer was dried over magnesium sulfate. After filtration to separate solvent and magnesium sulfate and precipitate, the solvent was removed under reduced pressure to give a residue, which was applied to a silica gel chromatography column and eluted with ethyl acetate/hexane =1/6 to furnish 4.9 g (96% yield) of the title compound as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214824B2
Source datasetuspto-grants-2007_05
ORD IDord-a2188f2deb3f47d280944600596765fc
Source noteuspto-grants-2007_05