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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170065Generated: November 2, 2026

Water → 4-(Benzyloxy)-2-tert-butylphenol

https://huagongshe.com/reaction/1170065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-ButylhydroquinoneHCID 16043—
Solvent2-MethoxyethanolHCID 8019—
Product4-(Benzyloxy)-2-tert-butylphenolHCID 12423646—

Reaction Steps

To a stirred solution of t-butyl hydroquinone (1.0 Kg) in 2-methoxy ethanol (2.0 L), was charged K2CO3 (2.0 Kg) portionwise under nitrogen atmosphere and the mixture refluxed. Benzyl chloride (0.762 L) was added dropwise at reflux temperature and heated further for 1.5 hr. The progress of the reaction was monitored on TLC. The reaction mixture was cooled and added DM Water (6.0 L). The uppermost oily layer was separated, dissolved in ethyl acetate (3.4 L), and washed with DM water (3.4 L×3). The uppermost oily layer was separated, dried over sodium sulfate and evaporated to dryness to give the crude title compound (1.5 Kg). The crude product was employed in the next step without further purification,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825257B1
Source datasetuspto-grants-2010_11
ORD IDord-af631e3ece794fdd851f76755404db6f
Source noteuspto-grants-2010_11