4-Methoxyphenol → Urethane acrylate

HRID 547877Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 547877
[CH2:1]([OH:23])[CH2:2][CH2:3]CCCCCCCCCCCCCCCCCCC.C(N=C=O)CCCCCN=C=[O:32].C1C=C(C[N:43]=[C:44]=[O:45])C=C(CN=C=O)C=1.C([O-])(=O)CCCCCCCCCCC.C([Sn+2]CCCC)CCC.C([O-])(=O)CCCCCCCCCCC.C(OCCO)(=O)C=C.COC1C=CC(O)=CC=1>C1(C)C=CC=CC=1>[C:1]([OH:23])(=[O:32])[CH:2]=[CH2:3].[NH2:43][C:44]([O:23][CH2:1][CH3:2])=[O:45]

Komponenten

8

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

Into 50 parts of toluene, 5.8 parts of behenyl alcohol (“NAA-422”, trade name, produced by NOF Corporation, hydroxyl value: 180) was added and the mixture was heated up to 40° C. After thorough dissolution of the behenyl alcohol, 50 parts of hexamethylene diisocyanate subjected to isocyanurate modification (“TAKENATE D-170N”) was added and the mixture was maintained at 70° C. for 30 minutes. Subsequently, 0.02 parts of dibutyltin laurate was added and the mixture was maintained at 70° C. for 3 hours. Further, 2.8 parts of 2-hydroxyethyl acrylate (Light Ester HOA), 36.1 parts of polycaprolactone-modified hydroxyethyl acrylate (“PLACCEL FA1”), 48.1 parts of polycaprolactone-modified hydroxyethyl acrylate (“PLACCEL FA5”), 0.02 parts of dibutyltin laurate and 0.02 parts of hydroquinone monomethyl ether were added and the mixture was maintained at 70° C. for 5 hours. Thereafter, 92.8 parts of toluene was added to obtain a urethane acrylate having a solid content of 50% by weight. The average number of repetitions per one molecule of the urethane acrylate relative to the number of repetitions of a caprolactone unit per one residue of an acrylate monomer is 2. Further, the maximum difference in the number of repetitions between two kinds of the urethane acrylates is 5.

Aufarbeitung

  1. additionwas added
  2. temperaturethe mixture was maintained at 70° C. for 30 minutes
  3. temperaturethe mixture was maintained at 70° C. for 3 hours
  4. temperaturethe mixture was maintained at 70° C. for 5 hours

Quellen und Nachweise

ORD-Eintrag
ord-322ffd5ad37a4837bd6265a5574f150c
Quelldatensatz
uspto-grants-2011_05
Patentnummer
US07939608B2

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