Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | 1,2-Epoxybutane | HCID 7834 | — |
| Reactant | Toluene 2,4-Diisocyanate | HCID 11443 | — |
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Product | Urethane acrylate | HCID 21863578 | — |
Reaction Steps
In a reaction vessel equipped with a stirrer, 109.8 gm of 2,4-tolylene diisocyanate, 1 gm of dibutyltindilaurate, and 0.3 gm of 2,6-di-t-butyl-4-methylphenol as a polymerization inhibitor were added. To this, 48.8 gm of hydroxyethylacrylate was added while controlling the temperature to 20° C. or lower. After the addition was completed the mixture was continuously stirred for an additional one hour at 10° to 20° C. Following this, 841.4 gm of a copolymerized diol of ethylene oxide and 1,2-butylene oxide [ethylene oxide:1,2-butylene oxide 1:9 (by weight)] of a number average molecular weight of 2,000 was added while maintaining the temperature in the 40° to 50° C. range, after which the mixture was continuously stirred for 5 hours at 50° to 60° C. to complete the reaction. A urethane acrylate [A-I] of a number average molecular weight of about 4,750 was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05496870 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-9d438753e6f44e6e8a8a80914fe2747f |
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| Source note | uspto-grants-1996_03 |
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