Dimethylformamide → Methacrylamide

HRID 1587465

Reaktionsgleichung

Reaktionsgleichung von HRID 1587465
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9]([O:14][CH:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1)(=[O:13])[C:10]([CH3:12])=[CH2:11].[C:21]([NH2:26])(=[O:25])[C:22]([CH3:24])=[CH2:23].CN(C)C=O>>[CH3:23][CH:22]1[CH2:24][CH:10]([CH3:11])[C:9](=[O:13])[NH:26][C:21]1=[O:25].[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9]([O:14][CH:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1)(=[O:13])[C:10]([CH3:12])=[CH2:11].[C:21]([NH2:26])(=[O:25])[C:22]([CH3:24])=[CH2:23]

Komponenten

8

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

A 2,4-dimethylglutarimide, styrene, and cyclohexyl methacrylate containing polymer was prepared by the techniques of copolymerization and glutarimidization. Accordingly an interpolymer of styrene, cyclohexyl methacrylate, and methacrylamide was prepared. In a 1.5 liter, glass reactor fitted with inlet tubes, nitrogen pad, and stirrer, styrene 29 g, cyclohexyl methacrylate 225 g, and methacrylamide 122 g, were introduced, along with 50 percent based o monomer weight of N,N-dimethylformamide solvent. 250 ppm of a peroxide initiator 1,1-bis(t-butylperoxy)cyclohexane was introduced and the reactor heated to 80-100° C. with stirring. Reaction was continued only a short time period (10-20 percent conversion) to prevent polymer compositional drift and possible degeneration of optical properties. The polymer was recovered by precipitation in methanol.

Aufarbeitung

  1. additionwere introduced, along with 50 percent
  2. customReaction
  3. customThe polymer was recovered by precipitation in methanol

Quellen und Nachweise

ORD-Eintrag
ord-16767af77c4f400e8ffc23813fb49c22
Quelldatensatz
uspto-grants-1993_06
Patentnummer
US05218068

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