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Formaldehyde → Benzoxazines

HRID 43227
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 43227
[CH2:1]=[O:2].[NH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:10]OCC(O)C>>[O:2]1[C:1]2[CH:10]=[CH:5][CH:6]=[CH:7][C:8]=2[CH:9]=[CH:4][NH:3]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 712FormaldehydeHCID 6115Aniline2×HCID 79001-Methoxy-2-propanol

Produkt 1

HCID 17845026Benzoxazines

Reaktionsbedingungen

Temperatur
105 °C

Versuchsvorschrift

The steps include: in a 2 L four-necked glass reactor equipped with a heating mantle, a temperature controller, an electric mixer and a condenser, 350 g of phenolic resin (C) having high proportion of tri-functional resin monomer and 246 g of paraformaldehyde are dissolved thoroughly in the presence of 816 g of a solvent propylene glycol monomethyl ether at 85° C., 334.4 g of aniline is dropped in the course of 3 hours into the reactor at constant speed by a quantitative pump to proceed the reaction at 85° C. After finishing the dropping addition of aniline, the temperature is kept at 85° C. for aging for 2 hours, then the temperature is raised to 105° C. After water and part of the solvent are removed, a benzoxazine resin solution with 56 wt % solid is obtained. According to gel permeation chromatography (GPC) analysis, the proportion of the tri-functional resin monomer in this benzoxazine resin is up to 60 area percent (Area %) or more.

Aufarbeitung

  1. customin a 2 L four-necked glass reactor equipped with a heating mantle
  2. customthe reaction at 85° C
  3. customis kept at 85° C.
  4. customAfter water and part of the solvent are removed

Quellen und Nachweise

ORD-Eintrag
ord-8ac4833d2bde4918a670d509dbef6cb0
Quelldatensatz
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08536283B2

Notizen zur Reaktion

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