Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | epsilon-CAPROLACTONE | HCID 10401 | — |
| Reactant | 1,6-Hexanediol | HCID 12374 | — |
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzylbenzene diisocyanate | HCID 19824838 | — |
| Product | Urethane acrylate | HCID 21863578 | — |
Reaction Steps
In a flask equipped with a thermometer, a stirrer and a condenser was charged 524 parts of diphenylmethane diisocyanate and heated to 60° C. with stirring. To the flask was added dropwise 520 parts of a ring opening reaction product (OH value: 215 KOH-mg/kg) between ε-caprolactone and 1,6-hexanediol over a period of 1 hour while giving care to heat generation. The reaction was carried on over 10 hours, and 232 parts of hydroxyethyl acrylate was added thereto, followed by further continuing the reaction for 10 hours. After confirming disappearance of the absorption of an isocyanate group in the infrared absorption spectrum, an urethane acrylate containing a hard segment and a soft segment was obtained as a comparative composition (designated RSH-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05714218 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-0c8b7b05f72c4fcb91b4a34bc79c5f07 |
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| Source note | uspto-grants-1998_02 |
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