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US4166828A Expired / Lapsed US ⏱️ 0.0 years remaining

Preparation of N-(aminomethyl)-α,β-ethylenically unsaturated carboxamides and their polymers

Assignee: Dow Chemical Co
•
Filing: 1977-12-02
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Granted: 1979-09-04
•
Expires: 1997-12-02
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Abstract

Abstract N-(aminomethyl)-α,β-ethylenically unsaturated carboxamides such as N-(dimethylaminomethyl)acrylamide are readily prepared without coincident production of saturated impurities by reacting an α,β-ethylenically unsaturated carboxamide such as acrylamide with a lower aldehyde such as formaldehyde and a secondary amine such as dimethylamine at a pH below 7. The resulting aminomethyl carboxamides are polymerized at a pH of 7 or less to form polymers containing essentially no gelled product.

Inventors

  • 👤 Charles J. McDonald

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 07:05
CPC Classifications
C; C08; C08F; C08F8/00; C08F8/44

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 127 words
A process for preparing a cationic N-(aminomethyl)-α,β-ethylenically unsaturated carboxamide which comprises contacting a reaction mixture comprising an α, β-ethylenically unsaturated carboxamide reactant with an aldehyde having 1 to 3 carbons and an amine represented by the structural formula: HN(R.sub.3).sub.2 wherein each R 3 is independently hydrocarbyl or both of R 3 are collectively a divalent hydrocarbon radical which combines with N of the amine to form a heterocyclic ring represented by the formula: ##STR5## under conditions including a pH of less than about 7 sufficient to cause reaction of the carboxamide reactant, aldehyde and amine to form at least 10 mole percent of the cationic carboxamide based on moles of the carboxamide reactant, provided that if the carboxamide reactant is acrylamide, the pH is less than 5.
Claim 2
Dependent Claim 127 words
A process for preparing a cationic N-(aminomethyl)-α,β-ethylenically unsaturated carboxamide which comprises contacting a reaction mixture comprising an α, β-ethylenically unsaturated carboxamide reactant with an aldehyde having 1 to 3 carbons and an amine represented by the structural formula: HN(R.sub.3).sub.2 wherein each R 3 is independently hydrocarbyl or both of R 3 are collectively a divalent hydrocarbon radical which combines with N of the amine to form a heterocyclic ring represented by the formula: ##STR5## under conditions including a pH of less than about 7 sufficient to cause reaction of the carboxamide reactant, aldehyde and amine to form at least 10 mole percent of the cationic carboxamide based on moles of the carboxamide reactant, provided that if the carboxamide reactant is acrylamide, the pH is less than 5.
Claim 3
Dependent Claim 66 words
The process of claim 1 wherein the carboxamide reactant is one represented by the formula: ##STR6## wherein R 1 is hydrogen or alkyl, R 2 is hydrogen or an inert substituent; and the cationic carboxamide is represented by the formula: ##STR7## wherein R 1 , R 2 and R 3 are as defined herein and R 4 is hydrogen or alkyl having one or two carbons.
Claim 4
Dependent Claim 31 words
The process of claim 2 wherein the ingredients of the reaction mixture are combined in an aqueous medium such that the pH of the reaction mixture is less than about 5.
Claim 5
Dependent Claim 26 words
The process of claim 2 wherein R 1 is hydrogen, methyl or ethyl, R 2 is hydrogen or alkyl, and R 3 is alkyl or alkenyl.
Claim 6
Dependent Claim 42 words
The process of claim 4 wherein the carboxamide reactant is acrylamide, the aldehyde is formaldehyde, or a material selected from paraformaldehyde, formalin and trioxymethane, the amine is a dialkylamine or diallylamine, and the pH of the reaction mixture is 3 or less.
Claim 7
Dependent Claim 35 words
The process of claim 2 wherein the reaction mixture is dissolved in an aqueous medium and dispersed in an oil phase to form a water-in-oil emulsion prior to the reaction to form the cationic carboxamide.

References Cited (Backward Citations)

US2328901A Cited
DE1102157B Cited
US3079434A Cited
US3178385A Cited
US3349121A Cited
FR1251025A Cited
US3171805A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-09-03 1983-03-05 1983-09-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-09-03 1987-03-05 1987-09-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-09-03 1991-03-05 1991-09-04 $7700.00 Window Closed / Lapsed

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