Potassium Carbonate → Diacetone acrylamide oxime

HRID 1703051Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1703051
[C:1]([NH2:5])(=O)[CH:2]=[CH2:3].[CH3:6][C:7]([CH3:9])=[O:8].[CH3:10][C:11]([CH3:13])=[O:12].Cl.[NH2:15][OH:16].C(=O)([O-])[O-].[K+].[K+]>O>[C:1](=[N:15][OH:16])([NH2:5])[CH:2]=[CH2:3].[CH3:6][C:7]([CH3:9])=[O:8].[CH3:10][C:11]([CH3:13])=[O:12]

Komponenten

5

Versuchsvorschrift

To a solution of 408 g. (2.4 moles) of diacetone acrylamide ##STR12## and 200 g. (2.88 moles; 20% molar excess) of hydroxylamine hydrochloride in 1.5 l. of distilled water was added a solution of 200 g. (1.44 moles) of potassium carbonate in 250 ml. of water at room temperature of about 25° C. over a period of 15 min. A precipitate formed after about 15 minutes. Stirring was continued until a thick paste formed and the mixture was then allowed to stand for another hour. The solid product was isolated by filtration, washed with small portions of water (amounting to a total of 500 ml.) and dried at 40° C. in a vacuum oven. Yield of 365 g. of a white crystalline powder (82% yield), m.p. 103° C. The material was of sufficient purity to be directly employed in polymerization and was employed in the polymerization described in Example 2 hereinafter. If desired, further purification can be attained through recrystallization from benzene or toluene.

Aufarbeitung

  1. customA precipitate formed after about 15 minutes
  2. customformed
  3. waitto stand for another hour
  4. customThe solid product was isolated by filtration
  5. washwashed with small portions of water (amounting to a total of 500 ml
  6. custom) and dried at 40° C. in a vacuum oven

Quellen und Nachweise

ORD-Eintrag
ord-648c20a8b2b74d7796dc575fd812d837
Quelldatensatz
uspto-grants-1982_09
Patentnummer
US04350801

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