Ammonia → 4-Acrylamido-4-methyl-2-pentanone

HRID 1390851

Reaktionsgleichung

Reaktionsgleichung von HRID 1390851
CC([NH:8][C:9](=[O:12])[CH:10]=[CH2:11])(C)[CH2:3][C:4](=[O:6])[CH3:5].N>O>[C:9]([NH2:8])(=[O:12])[CH:10]=[CH2:11].[CH3:3][C:4]([CH3:5])=[O:6].[CH3:3][C:4]([CH3:5])=[O:6]

Komponenten

4

Edukt 2

HCID 222AmmoniaHCID 17888N-(1,1-Dimethyl-3-oxobutyl)acrylamide

Produkt 1

HCID 215849214-Acrylamido-4-methyl-2-pentanone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A process is disclosed for preparing N-(1,1-dimethyl-3-oxobutyl)acrylamide which comprises (1) contacting a dispersion of 5,6-dihydro-6-hydroxy-4,4,6-trimethyl-2-vinyl-1,3,3(4H)-oxazine-3-ium sulfate (1:1) in a water-immiscible organic solvent with a neutralizing or alkalizing amount of gaseous ammonia at a temperature between about 10° C. and 25° C. to form a solution of diacetone acrylamide in said organic solvent and a precipitate of crystalline ammonium sulfate; (2) separating the crystals of ammonium sulfate; (3) cooling the organic mother liquors recovered from step (2) to about -10° C. to 20° C. to crystallize N-(1,1-dimethyl-3-oxobutyl)acrylamide therefrom; and (4) recovering the crystals of N-(1,1-dimethyl-3-oxabutyl) acrylamide, washing the recovered crystals with a cold water-immiscible organic solvent and drying the same.

Aufarbeitung

  1. customat a temperature between about 10° C. and 25° C.

Quellen und Nachweise

ORD-Eintrag
ord-98b4b16063fe4c1b862eb1f8ada47619
Quelldatensatz
uspto-grants-1979_02
Patentnummer
US04140715

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