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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090607Generated: October 27, 2026

1-Bromohexane → 4-Hexyloxyphenol

https://huagongshe.com/reaction/1090607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexaneHCID 8101—
ReactantSodium hydrideHCID 24758—
Reactant2-(Phenylmethyl)-1,4-benzenediolHCID 74354—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-HexyloxyphenolHCID 2935477.2%

Reaction Steps

Sodium hydride (2.4 g, 0.1 mol) was suspended in 150 mL dry glyme. Monobenzylhydroquinone (20.0 g, 0.1 mol) was dissolved in 250 mL dry glyme and added dropwise to the sodium hydride suspension with stirring under nitrogen at room temperature. 1-Bromohexane (16.5 g, 0.1 mol) was added dropwise and the reaction mixture was refluxed for 1 day. The reaction product was cooled and the glyme removed under reduced pressure. The residue was dissolved in 300 mL 1:1 ethanol-ethyl acetate and catalytically hydrogenated using 2 g 10% Pd on C and a hydrogen pressure of 500 kPa at room temperature for 4 hours. The catalyst was removed by filtration and the solvent was removed from the filtrate under reduced pressure. The crude product residue was recrystallized from aqueous ethanol to yield 15 g 4-hexyloxyphenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082587
Source datasetuspto-grants-1992_01
ORD IDord-ad1bd2e683a8449290805f1379168609
Source noteuspto-grants-1992_01