Modification chloroacetic acid

Protocol for the Modification of Dextran with Chloroacetic Acid... 

The following protocol illustrates the modification of a dextran polymer with chloroacetic acid. 

Hydrophilic polystyrene-based continuous beds bearing a hydrophilic surface on a hydrophobic polymeric support were prepared by a two-step modification of polychloromethylstyrene monolith first with ethylenediamine followed either by a reaction with y-gluconolactone or with chloroacetic acid [57,122]. Activation could also be performed by grafting 4-vinyl-2,2-dimethylazactone onto the monolith porous surface [123]. 

It is necessary that each type have a name, that this name be conserved in all of the numerous modifications it can undergo. On this principle I have already formed the names acetic and chloroacetic acid, ether and chloroether—names with an aim at recalling the persistence of types in spite of the intervention of chlorine in these compounds. 

Condensation of salicylaldehyde and its derivatives with a variety of esters of chloroacetic acids in the presence of TBAB led to the synthesis of benzo[b]furans by means of a solid-liquid PTC reaction under the action of microwave irradiation [39]. This was a modification of one of the most popular routes to substituted benzo[b]furans, i.e. O-alkylation of O-hydroxylated aromatic carbonyl compounds with a-halogenated carbonyl compounds then intramolecular condensation. The mixture of aldehydes and chloroacetic acid esters were absorbed on potassium carbonate then irradiated in an open vessel in a domestic MW oven for 8-10 min (Eq. 26). 

Chemical. A large number of chitin and chitosan derivatives have been synthesized through modification of the primary (C-6) and secondary (C-3) hydroxyl groups present on each repeat imit, including amine (C-2) functionality existing on deacetylated imits (31). Reactions typical of hydroxyl and amine groups (such as acylations with acid chlorides and anhydrides) including urethane and urea formation respectively, are feasible with isocyanates. The primary amine can be quatemized by alkyl iodides or converted to an imine with a variety of aldehydes and ketones that can subsequently be reduced to an N-alkylated derivative. Chitin and chitosan are reactive with a variety of alkyl chlorides after treatment with concentrated NaOH. Important derivatives such as carboxymethylated chitin and chitosan are commonly produced in this manner with the addition of sodium chloroacetate. 

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