関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethylene Oxide | HCID 6354 | — |
| 反応物 | 1,2-Epoxybutane | HCID 7834 | — |
| 反応物 | Toluene 2,4-Diisocyanate | HCID 11443 | — |
| 反応物 | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| 反応物 | (3-Mercaptopropyl)trimethoxysilane | HCID 20473 | — |
| 反応物 | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| 反応物 | Isocyanate | HCID 105034 | — |
| 生成物 | Urethane acrylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06309747B1 |
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| 出典データセット | uspto-grants-2001_10 |
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| ORD ID | ord-2d7d25fff42c4f5381d01eeb862b67d5 |
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| 出典メモ | uspto-grants-2001_10 |
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