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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259794Generated: October 26, 2026

Acrylic Acid → Urethane acrylate

https://huagongshe.com/reaction/2259794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylic AcidHCID 6581—
Reactant2-Hydroxyethyl acrylateHCID 13165—
Reactant2-Hydroxy-2-methyl-1-phenylpropan-1-oneHCID 81984—
ReactantIsocyanateHCID 105034—
ReactantDi-n-butyldilauryltinHCID 9809426—
ReactantIsobomyl acrylateHCID 92004758—
SolventEthanolHCID 702—
SolventTetrahydrofurfuryl acrylateHCID 94232—
ProductUrethane acrylateHCID 21863578—

Reaction Conditions

Temperature80 °C

Reaction Steps

An acrylate urethane oligomer composition was prepared in the following manner. A flask was charged with 202.8 g of PPG 1025 (polypropylene glycol with average molecular weight of 1025), 83.2 g of PPG 425 (polypropylene glycol with average molecular weight of 425), 221.6 g of isobornyl acrylate, 150.0 g of diphenylmethane 4,41 diisocyanate and 0.4 g of dibutyltin dilaurate. The mixture was heated at 80° C. for two hours. Hydroxyethyl acrylate, 23.2 g, was added and the heating continued for one hour. Ethanol, 9.7 g, was added and heating continued until the isocyanate band in the IR at 2268 cm-1 disappeared. The still warm product was diluted with 211.6 g of tetrahydrofurfuryl acrylate, 35.2 g acrylic acid and 35.2 g of Darocure 1173 initiator which is 2-hydroxy-2-methyl-1-phenyl-propane-1-one, a product of Ciba-Geigy. After thoroughly mixing, the mixture was poured warm into an opaque container. The yield of colorless product was 973 g with a viscosity of 8100 cP.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475038
Source datasetuspto-grants-1995_12
ORD IDord-c4c9dd2e963747218d6ab6f32af6e9ea
Source noteuspto-grants-1995_12