2-Hydroxyethyl acrylate → Urethane acrylate
反応式
[N-:1]=[C:2]=[O:3].[N-]=C=O.[O:7]=[C:8]1CC(C)(C)CC(C)=[CH:9]1.FC(F)(F)C(C1CCC(O)CC1)(C1CCC(O)CC1)C(F)(F)F.[C:40]([O:44]CCO)(=[O:43])[CH:41]=[CH2:42]>CC(C)=O.C([O-])(=O)CCCCCCCCCCC.C([O-])(=O)CCCCCCCCCCC.C([Sn+2]CCCC)CCC.COC1C=CC(O)=CC=1>[C:40]([OH:44])(=[O:43])[CH:41]=[CH2:42].[NH2:1][C:2]([O:7][CH2:8][CH3:9])=[O:3]参加物
実験手順
In 300 g of acetone were dissolved 46.2 g of isophoronediisocyanate, 70.3 g of 4,4'-(perfluoroisopropylidene)dicyclohexanol and 0.8 g of di-n-butyltin dilaurate. The mixture was reacted at 54° to 56° C. for 15 hours with stirring while introducing dry nitrogen. To the mixture were added 10 g of 2-hydroxyethyl acrylate, 0.4 g of di-n-butyltin dilaurate and 0.1 g of hydroquinone monomethyl ether and the mixture was reacted at 54° to 56° C. for 16 hours. A few drops of the reaction mixture were placed on KBr plate. The plate was dried and subjected to infrared absorption spectrum analysis to find an absorption based on isocyanate group (2250 cm-1) disappeared. The reaction mixture was poured into a large excess amount of hexane and the resulting precipitates were filtered, dried and pulverized to obtain 114 g of urethane acrylate in the form of white powder.
後処理
- customThe mixture was reacted at 54° to 56° C. for 15 hours
- additionwhile introducing dry nitrogen
- customthe mixture was reacted at 54° to 56° C. for 16 hours
- customThe plate was dried
- customan absorption
- additionThe reaction mixture was poured into a large excess amount of hexane
- customthe resulting precipitates
- filtrationwere filtered
- customdried
出典と根拠
- ORDレコード
- ord-e0176e71a351451480f0d2f604d40f58
- 出典データセット
- uspto-grants-1988_11
- 特許番号
- US04788327
反応ノート
読み込み中…