C07C57/66

RECYCLABLE CATALYSTS FOR CHLORINATION OF ORGANIC ACIDS AND ALCOHOLS

The present invention discloses recyclable polymeric catalyst of Formula I, for chlorination of organic acids and alcohols using chlorinating agents such as carbonyl chloride, oxalyl chloride or thionyl chloride,

##STR00001##

wherein, ‘m’ on the pendent groups on polystyrene backbone can have values from 1 to 5 and R is the alkyl group ranging from C1 to C5.

RECYCLABLE CATALYSTS FOR CHLORINATION OF ORGANIC ACIDS AND ALCOHOLS

The present invention discloses recyclable polymeric catalyst of Formula I, for chlorination of organic acids and alcohols using chlorinating agents such as carbonyl chloride, oxalyl chloride or thionyl chloride,

##STR00001##

wherein, ‘m’ on the pendent groups on polystyrene backbone can have values from 1 to 5 and R is the alkyl group ranging from C1 to C5.

PROCESS FOR PREPARING FATTY ACID CHLORIDES AND N-ACYL AMINO ACID SALTS

The invention relates to a process for preparing fatty acid chlorides. In a subsequent step, the fatty acid chlorides can be used to prepare N-acyl amino acid salts. The process comprises the formation of a fatty acid chloride in an amine catalyzed reaction of a fatty acid with phosphorous trichloride, thionyl chloride or phosgene, preferably thionyl chloride. The process for preparing N-acyl amino acid salts further comprises the reaction of the fatty acid chloride with an amino acid or an amino ethane sulfonic acid.

PROCESS FOR PREPARING FATTY ACID CHLORIDES AND N-ACYL AMINO ACID SALTS

The invention relates to a process for preparing fatty acid chlorides. In a subsequent step, the fatty acid chlorides can be used to prepare N-acyl amino acid salts. The process comprises the formation of a fatty acid chloride in an amine catalyzed reaction of a fatty acid with phosphorous trichloride, thionyl chloride or phosgene, preferably thionyl chloride. The process for preparing N-acyl amino acid salts further comprises the reaction of the fatty acid chloride with an amino acid or an amino ethane sulfonic acid.

Process for preparing fatty acid chlorides and N-acyl amino acid salts

The invention relates to a process for preparing fatty acid chlorides. In a subsequent step, the fatty acid chlorides can be used to prepare N-acyl amino acid salts. The process comprises the formation of a fatty acid chloride in an amine catalyzed reaction of a fatty acid with phosphorous trichloride, thionyl chloride or phosgene, preferably thionyl chloride. The process for preparing N-acyl amino acid salts further comprises the reaction of the fatty acid chloride with an amino acid or an amino ethane sulfonic acid.

Process for preparing fatty acid chlorides and N-acyl amino acid salts

The invention relates to a process for preparing fatty acid chlorides. In a subsequent step, the fatty acid chlorides can be used to prepare N-acyl amino acid salts. The process comprises the formation of a fatty acid chloride in an amine catalyzed reaction of a fatty acid with phosphorous trichloride, thionyl chloride or phosgene, preferably thionyl chloride. The process for preparing N-acyl amino acid salts further comprises the reaction of the fatty acid chloride with an amino acid or an amino ethane sulfonic acid.

Monomers and polymers formed thereby

Monomers, polymers, or oligomers formed therefrom and methods of forming or utilizing monomers of formula I ##STR00001##
where R.sup.1 is a C.sub.1 to C.sub.4 alkyl; and X is —OH; —OM where M is lithium (Li), sodium (Na), or potassium (K), NH.sub.4.sup.+, R.sup.5NH.sub.3.sup.+, R.sup.5.sub.2NH.sub.2.sup.+, R.sup.5.sub.3NH.sup.+, R.sup.5.sub.4N.sup.+ where R.sup.5 can independently be selected from alkyl, benzyl, and combinations thereof; —OR.sup.2 where R.sup.2 can be a C.sub.1 to C.sub.4 alkyl, 2-ethylhexyl, or a hydrocarbon moiety of bio-renewable alcohol or a hydrogenated derivative thereof; —NR.sup.3R.sup.4, —NR.sup.3—NR.sup.3R.sup.4, —NR.sup.3—OR.sup.4 where R.sup.3 and R.sup.4 can independently be H, a C.sub.1 to C.sub.4 alkyl, or combinations thereof.

Monomers and polymers formed thereby

Monomers, polymers, or oligomers formed therefrom and methods of forming or utilizing monomers of formula I ##STR00001##
where R.sup.1 is a C.sub.1 to C.sub.4 alkyl; and X is —OH; —OM where M is lithium (Li), sodium (Na), or potassium (K), NH.sub.4.sup.+, R.sup.5NH.sub.3.sup.+, R.sup.5.sub.2NH.sub.2.sup.+, R.sup.5.sub.3NH.sup.+, R.sup.5.sub.4N.sup.+ where R.sup.5 can independently be selected from alkyl, benzyl, and combinations thereof; —OR.sup.2 where R.sup.2 can be a C.sub.1 to C.sub.4 alkyl, 2-ethylhexyl, or a hydrocarbon moiety of bio-renewable alcohol or a hydrogenated derivative thereof; —NR.sup.3R.sup.4, —NR.sup.3—NR.sup.3R.sup.4, —NR.sup.3—OR.sup.4 where R.sup.3 and R.sup.4 can independently be H, a C.sub.1 to C.sub.4 alkyl, or combinations thereof.

Linker compounds, methods of producing the same and uses thereof

The present disclosure provides a bifunctional linker for coupling at least one functional moiety, preferably a bis-allyl propionic acid (BAPA), to a polymer-containing matrix. Also disclosed by the present disclosure are anhydrides of the bifunctional linker, processes for preparing the bifunctional linker and such anhydride, as well as surfaces, such as cellulose containing matrices, coupled with the bifunctional linker, at times, the latter carrying a functional agent.

Linker compounds, methods of producing the same and uses thereof

The present disclosure provides a bifunctional linker for coupling at least one functional moiety, preferably a bis-allyl propionic acid (BAPA), to a polymer-containing matrix. Also disclosed by the present disclosure are anhydrides of the bifunctional linker, processes for preparing the bifunctional linker and such anhydride, as well as surfaces, such as cellulose containing matrices, coupled with the bifunctional linker, at times, the latter carrying a functional agent.