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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726481Generated: October 25, 2026

Tetrahydrofuran → 2-(Acryloyloxyethoxy)phenol acrylate

https://huagongshe.com/reaction/726481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant2-(2-Hydroxyethoxy)phenolHCID 78519—
CatalystPhenothiazineHCID 7108—
Product2-(Acryloyloxyethoxy)phenol acrylateHCID 5432006162%

Reaction Steps

A 500-ml, two necked flask was equipped with magnetic stirring bar, nitrogen atmosphere and an addition funnel. The flask was charged with 25 g of 2-(2-hydroxyethoxy)phenol (0.16 mol.), 33 g of triethylamine (0.32 mol.), 250 ml of tetrahydrofuran and 1 g of phenothiazine. Next, 30 g of acryloyl chloride (0.18 mol.) was slowly added to the reaction over 1 hour via the addition funnel. The triethylamine hydrochloride salt was removed by filtration and the mother liquor was evaporated with a rotoevaporator. The remaining liquid was dissolved in chloroform and washed with NaCl(aq.), NH4OH(10%), NaCl(aq.) and dried over MgSO4. The chloroform was removed with a rotoevaporator to yield 26 g (62%) of a reddish brown liquid. The product was confirmed by IR and 13C NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05709935
Source datasetuspto-grants-1998_01
ORD IDord-4b28f6d0330a43b2b8eaee022e05f177
Source noteuspto-grants-1998_01