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HRID 382221作成日:2026年10月24日

Ethylene Oxide → Urethane acrylate

https://huagongshe.com/reaction/382221

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene OxideHCID 6354—
反応物1,2-EpoxybutaneHCID 7834—
反応物Toluene 2,4-DiisocyanateHCID 11443—
反応物2-Hydroxyethyl acrylateHCID 13165—
反応物(3-Mercaptopropyl)trimethoxysilaneHCID 20473—
反応物2,6-Di-tert-butyl-4-methylphenolHCID 31404—
反応物IsocyanateHCID 105034—
生成物Urethane acrylateHCID 21863578—

反応手順

Into a reaction vessel equipped with a stirrer were charged 3.0 parts of tolylene diisocyanate, 50.5 parts of a ring-opening copolymer from ethylene oxide and butene oxide, having a number average molecular weight of 4,000, and 0.01 part of 2,6-di-t-butyl-p-cresol, as a polymerization inhibitor. The mixture was cooled with ice to a temperature of below 10° C., while stirring. When the temperature was lower than 10° C., 0.04 part of dibutyltindilaurate was added and the mixture was stirred for 2 hours while controlling the temperature at 20-30° C. Then, after the addition of 0.3 part of γ-mercaptopropyltrimethoxy silane, the mixture was stirred for a further one hour at 30-40° C., whereupon 1.2 parts of hydroxyethyl acrylate was added. The mixture was stirred for 4 hours at 50-60° C., until the amount of remaining isocyanate is 0.1% by weight or less. The liquid urethane acrylate obtained in this manner is hereinafter referred to as UA-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06309747B1
出典データセットuspto-grants-2001_10
ORD IDord-2d7d25fff42c4f5381d01eeb862b67d5
出典メモuspto-grants-2001_10