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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488481Generated: October 28, 2026

2-Hydroxyethyl acrylate → HCID 21225502, compound

https://huagongshe.com/reaction/488481

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxyethyl acrylateHCID 13165—
ReactantIsocyanateHCID 105034—
ReactantIsophorone diisocyanateHCID 169132—
ProductHCID 21225502HCID 212255022,150.1%

Reaction Steps

A 250 mL, 3 neck round bottom flask fitted with a mechanical stirrer and a thermometer was dried under nitrogen and charged with poly-7-FOX diol (polyfluorooxetane diol with heptafluoro group) (24.3 grams, 9.1 meq.) from Example 5. Isophorone diisocyanate (3.0 grams, 27.2 meq) and dibutyltindilaurate (12 mg) were added and the mixture was heated at 70 C for 14 hours. The reaction mixture was cooled to room temperature and washed with heptane (2 times 100 mL each). The isocyanate-terminated poly-7-FOX prepolymer was then dissolved in tetrahydrofuran (50 mL) and treated with dibutyltin dilaurate (12 mg). The resulting solution was reacted with 2-hydroxyethyl acrylate (HEA, 1.16 gram, 10 meq) at room temperature. No observable exotherm was observed on the addition of HEA. The progress of the reaction was monitored by following the disappearance of the isocyanate band in an infrared spectroscopic spectrum (IR) at 2270 cm−1. The mixture was heated at a temperature of 60 C for 4 hours. On completion, as indicated by the disappearance of the NCO band in the IR, the reaction mixture was precipitated into water (450 mL). The resulting solution was dried over magnesium sulfate, filtered and stripped of solvent under reduced pressure to produce 17.2 grams of a urethane-acrylate terminated poly-7-FOX.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06972317B2
Source datasetuspto-grants-2005_12
ORD IDord-73c6db57416b4f8b99f7375e16dc03ba
Source noteuspto-grants-2005_12