Hydrochloric Acid → HCID 86741663, compound
Reaction equation
[ClH:1].[CH:2]([CH:6]=[CH:7][CH2:8][NH2:9])([CH2:4][CH3:5])[CH3:3]>>[ClH:1].[CH:2]([CH:6]=[CH:7][CH2:8][NH2:9])([CH2:4][CH3:5])[CH3:3]Participants
Procedure
While cooling the reaction mixture, 52.1 g of 35% hydrochloric acid was added to 56.6 g (0.5 mole) of N-sec-butylallylamine to obtain 108.7 g of a 68.84% aqueous solution of N-sec-butylallylamine hydrochloride (hereinafter, abbreviated as s-BAA.HCl). After diluting 21.74 g (0.1 mole) of the latter solution with 13.98 g of water, 16.17 g of dimethyldiallylammonium chloride (hereinafter, abbreviated as DMDA AmCl) was dissolved thereinto to prepare an aqueous solution having a monomer concentration of 60%. After heating the solution to 60° C., 0.934 g of 2,2'-azobis(2-amidinopropane) dihydrochloride was added as a polymerization initiator, and a polymerization reaction was carried out at that temperature for 48 hours. After the reaction, the reaction mixture (a solution) was poured into a large amount of acetone to precipitate the reaction product. The precipitate was collected by filtration using a glass filter and then dried under reduced pressure. Thus, a copolymer of N-sec-butylallylamine hydrochloride and dimethyldiallylammonium chloride was obtained.
Sources & evidence
- ORD record
- ord-f6cf6c0baede43358b3b4bdff8fe5d31
- Source dataset
- uspto-grants-1987_07
- Patent number
- US04678474
Reaction notes
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