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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28315Generated: October 25, 2026

4-Hydroxybenzyl Alcohol → 6-[4-(Hydroxymethyl)phenoxy]hexyl prop-2-enoate

https://huagongshe.com/reaction/28315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantPotassium CarbonateHCID 11430—
ReactantAcrylic acid 6-iodohexyl esterHCID 11289038—
SolventDimethylformamideHCID 6228—
Product6-[4-(Hydroxymethyl)phenoxy]hexyl prop-2-enoateHCID 23448422—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture consisting of 2.48 g of 4-hydroxybenzylalcohol, 5.64 g of 6-iodohexyl acrylate, and 2.76 g of potassium carbonate in 50 ml of DMF was stirred under nitrogen atmosphere for 3 h at 60° C. After being cooled to room temperature the reaction mixture was quenched with 100 ml 3N HCl and extracted with diethylether (2×100 ml). The combined ether extracts were washed with saturated NaCl solution, dried over sodium sulphate and concentrated to dryness to give 5.3 g of nearly pure 4-(6-acryloyloxyhexyloxy)benzylalcohol as a beige heavy oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07419620B2
Source datasetuspto-grants-2008_09
ORD IDord-baca2d09bcd849169359f86b1ed8d54e
Source noteuspto-grants-2008_09