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
To a reaction vessel equipped with a stirrer, 233.1 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 was added. To this, 250.6 gm of 2-hydroxyethylacrylate was added while controlling the temperature to 20° C. or less. After the addition was completed the mixture was continuously stirred for an additional one hour at 10° to 20° C. Following this, 516.8 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-4] of a number of average molecular weight of about 1,850 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-bb1f6c118357423ba905e0f117f42ed9 |
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| Source note | uspto-grants-1996_03 |
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