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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650645Generated: November 1, 2026

Chlorohydroquinone → 4-Dodecyloxybenzyl(4-hydroxy-2-chlorophenyl) ether

https://huagongshe.com/reaction/1650645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorohydroquinoneHCID 301—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-(Bromomethyl)-4-(dodecyloxy)benzeneHCID 23052179—
Product4-Dodecyloxybenzyl(4-hydroxy-2-chlorophenyl) etherHCID 56975878—

Reaction Steps

In an aqueous solution of sodium hydroxide, 2.0 g of 4-dodecyloxybenzyl bromide synthesized in the same manner as described in Referential Example 17 was reacted under reflux with 1.0 g of 4-hydroxy-3-chlorophenol for 8 hours, the thus-obtained solution was put into ice-cooled hydrochloric acid, and the precipitate was recovered by filtration, washed, dried and purified by the silica gel column chromatography to obtain 0.8 g of 4-dodecyloxybenzyl(4-hydroxy-2-chlorophenyl) ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925591
Source datasetuspto-grants-1990_05
ORD IDord-01eaf141db0c4242a015161c5ff95c91
Source noteuspto-grants-1990_05