2-Hydroxyethyl Methacrylate → 2-Ethyl-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid

HRID 536913

Reaktionsgleichung

Reaktionsgleichung von HRID 536913
C[C@@]12[CH:10]([C:11]([C:13]([O-:15])=[O:14])=C)C[C@H](C1(C)C)CC2.[C:16]([O:20]C[CH:22]1[O:26][CH2:25][CH2:24][CH2:23]1)(=[O:19])[CH:17]=[CH2:18].[C:27]([O:32]CCO)(=[O:31])[C:28](C)=[CH2:29].[C:36](OCCCCCCOC(=O)C=C)(=[O:39])C=C>>[C:13]([OH:15])(=[O:14])[CH:11]=[CH2:10].[C:16]([OH:20])(=[O:19])[CH:17]=[CH2:18].[C:27]([OH:32])(=[O:31])[CH:28]=[CH2:29].[CH2:36]([C:23]([CH2:22][OH:26])([CH2:13][OH:15])[CH2:24][CH3:25])[OH:39]

Komponenten

5

Edukt 4

HCID 133602-Hydroxyethyl MethacrylateHCID 256441,6-Hexanediol diacrylateHCID 94232Tetrahydrofurfuryl acrylateHCID 92004758Isobomyl acrylate

Produkt 1

HCID 250191762-Ethyl-2-(hydroxymethyl)propane-1,3-diol;prop-2-enoic acid

Versuchsvorschrift

Using the compositions obtained in Examples 2 to 5 and 7, the following mixture was prepared. That is, the mixture of 100 g (content of fine polymer particles: 5 g) in total, composed of the composition of 7.7 g of Example 2, isobornyl acrylate of 56.35 g, the composition of 5 g of Example 3, tetrahydrofurfuryl acrylate of 0.5 g, the composition of 2 g of Example 4, hydroxyethyl methacrylate of 8 g, the composition of 5 g of Example 5, 1,6-hexanediol diacrylate of 5.25 g, the composition of 5 g of Example 7 and trimethylolpropane triacrylate of 5.2 g was prepared.

Aufarbeitung

  1. customobtained in Examples 2 to 5 and 7
  2. customthe following mixture was prepared
  3. additionthe mixture of 100 g (content of fine polymer particles: 5 g) in total

Quellen und Nachweise

ORD-Eintrag
ord-547a40ca60134d2cba79d7a7bf4430d1
Quelldatensatz
uspto-grants-2014_10
Patentnummer
US08859642B2

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