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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078766Generated: November 1, 2026

Acrylic Acid → Acrylic Acid

https://huagongshe.com/reaction/2078766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylic AcidHCID 6581—
ReactantButyl AcrylateHCID 8846—
Reactant2-Hydroxyethyl acrylateHCID 13165—
SolventEthyl AcetateHCID 8857—
ProductAcrylic AcidHCID 6581—
ProductButyl AcrylateHCID 8846—
Product2-Hydroxyethyl acrylateHCID 13165—
ProductAcrylateHCID 25188—

Reaction Steps

100 parts by weight of butyl acrylate, 5 parts by weight of acrylic acid, 0.075 parts by weight of 2-hydroxyethyl acrylate, 0.3 parts by weight of 2,2-azobisisobutyronitrile, and ethyl acetate were added to a reactor vessel equipped with a cooling tube, a nitrogen introducing tube, a thermometer, and a stirrer so that a solution was formed. While nitrogen gas was blown into the solution, the solution was then subjected to a polymerization reaction at 60° C. for 4 hours to give an acrylate copolymer of butyl acrylate, acrylic acid and 2-hydroxyethyl acrylate with a weight average molecular weight of 2,200,000. The acrylate copolymer was diluted with ethyl acetate to form a polymer solution (2-A) with a total solids content of 30% by weight. To the polymer solution (2-A) were then added 0.6 parts by weight of a crosslinking agent mainly composed of an isocyanate group-containing compound (“Coronate L” (trade name) manufactured by Nippon Polyurethane Industry Co., Ltd.) and 0.075 parts by weight of γ-glycidoxypropyltrimethoxysilane (“KBM-403” (trade name) manufactured by Shin-Etsu Chemical Co., Ltd.) in this order, based on 100 parts by weight of the acrylate copolymer, so that a polymer solution (2-B) was prepared.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07929086B2
Source datasetuspto-grants-2011_04
ORD IDord-f043251ccd974c56ac3b621b3fd15f6a
Source noteuspto-grants-2011_04