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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439808Generated: November 1, 2026

Methacrylic Acid → Bisphenol A

https://huagongshe.com/reaction/1439808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacrylic AcidHCID 4093—
ReactantAcrylic AcidHCID 6581—
ReactantGlycidyl acrylateHCID 7836—
ReactantGlycidyl methacrylateHCID 7837—
ReactantAllyl glycidyl etherHCID 7838—
ReactantAcryloyl chlorideHCID 13140—
Reactant((o-Allylphenoxy)methyl)oxiraneHCID 98437—
ReactantMethallyl glycidyl etherHCID 13668594—
ReactantCrotyl phenyl glycidyl etherHCID 131710954—
ProductBisphenol AHCID 6623—
ProductEpichlorohydrinHCID 7835—

Reaction Steps

Examples of the compound having an effectively photopolymerizable carbon-to-carbon double bond and a 1,2-epoxy group in the molecule and having a boiling point of at least 120° C. [component (B) (i)] are glycidyl acrylate, glycidyl methacrylate, glycidyl allyl ether, o-allyl phenyl glycidyl ether, crotyl phenyl glycidyl ether, methallyl glycidyl ether, epoxy acrylate type resins obtained by condensing a part of the epoxy group of the polyepoxy compound exemplified above as component (A) with acrylic acid or methacrylic acid, epoxy acrylate type resins obtained by adding acryloyl chloride to the side chain of the polyepoxy compound exemplified above as component (A), especially an epoxy resin obtained by the condensation of bisphenol A and epichlorohydrin, and polyepoxy compounds obtained by epoxidizing some of the many carbon-to-carbon double bonds present in polybutadiene obtained by anionic polymerization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04060656
Source datasetuspto-grants-1977_11
ORD IDord-08435dfe3bbf460099b988bf5a9276c2
Source noteuspto-grants-1977_11