참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methoxyphenol | HCID 9015 | — |
| 반응물 | Toluene 2,4-Diisocyanate | HCID 11443 | — |
| 반응물 | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| 반응물 | CID 3084433 | HCID 3084433 | — |
| 반응물 | Di-n-butyl diacetoxy tin | HCID 9798523 | — |
| 생성물 | Urethane acrylate | HCID 21863578 | — |
반응 단계
In a flask equipped with a stirring blade, 348 parts (2 mol) of TDI (2,4-tolylene diisocyanate) was charged and 2000 parts (1 mol) of polytetramethylene glycol (number-average molecular weight of 2000) and dibutyltin diacetate were added while stirring. After heating to 70° C. while paying attention to heat generation, 0.2 parts of p-methoxyphenol and 1 part of 2,6-tertiary butyl-4-methylphenol were added. The reaction was conducted at the same temperature for 7 hours. Then, 232 parts (2 mol) of HEA (2-hydroxyethyl acrylate) was charged and the reaction was further reacted at the same temperature for 7 hours. After confirming the disappearance of absorption of NCO by infrared absorption spectrum, the reaction product was taken out to obtain a urethane acrylate (OS-2) as a radical polymerizable oligomer (A1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06850682B2 |
|---|
| 출처 데이터셋 | uspto-grants-2005_02 |
|---|
| ORD ID | ord-f11f8053711e4953b6065402e5c5130e |
|---|
| 출처 메모 | uspto-grants-2005_02 |
|---|
