Succinic acid amines

Corrosion inhibitors partial esters of succinic acid, fatty acids, sulfonates, phenates, amine phosphates. 

Finally, when polyamides containing four or five carbon diacids, ie, succinic acid [110-15-6] and glutaric acid [110-94-1], respectively, are heated, they form cychc imides that cap the amine ends and prevent high molecular weights from being achieved (84). For nylon-x,4, n = 1 and for nylon-x,5, n = 2. 

V-Phenylsuccinimide [83-25-0] (succanil) is obtained in essentially quantitative yield by heating equivalent amounts of succinic acid and aniline at 140—150°C (25). The reaction of a primary aromatic amine with phosgene leads to formation of an arylcarbamoyl chloride, that when heated loses hydrogen chloride to form an isocyanate. Commercially important isocyanates are obtained from aromatic primary diamines. 

Succinic acid reacts with urea in aqeous solution to give a 2 1 compound having mp 141°C (116,117), which has low solubiUty in water. A method for the recovery of succinic acid from the wastes from adipic acid manufacture is based on this reaction (118,119). The monoamide succinamic acid [638-32-4] NH2COCH2CH2COOH, is obtained from ammonia and the anhydride or by partial hydrolysis of succinknide. The diamide succinamide [110-14-3], (CH2C0NH2)2, nip 268—270°C, is obtained from succinyl chloride and ammonia or by partial hydrolysis of succinonitrile. Heating succinknide with a primary amine gives A/-alkylsucckiknides (eq. 9). 

It is important to emphasize that the introduction of a spacer should never affect the binding characteristics of the support. The selected spacer must not introduce any charges and should not be sufficiently hydrophobic to cause any kind of non-specific interaction. Several molecules can fulfill this demand but only a few of them are regularly used. Most of these contain terminal amino or carboxylic groups. In particular these are diaminodipropyl amine, 6-aminocapronic acid, 1,6-diaminohexane, ethylenediamine, l,3-diamino-2-propanol, succinic acid, 1,4-butanediol diglycidyl ether, and others [96]. Extensive description of other bifunctional reagents can be found in the book of Wong [89]. 

Figure 15 Examples of artificial collagen model peptide knots, (a) Regioselective artificial cystine knot, (b) dilysine scaffold,(c) c/s,c/s-1,3,5-trimethylcyclohexane-1,3,5-tricarboxylic acid Kemp tri acid , (d) TREN-(suc-OH)3, (Tris(2-aminoethyl)amine) succinic acid, (e) Fe + [2,2 -bipyridyl-peptide]3, " (f) monoalkyl chains, " (g) Boc-/3-Ala-TRIS-(OH)3 knot, and (h) N-terminal GFGEEG link. ...

Figure 4.28. The skeleton model for succinic acid, P-alanine, and ethane diamine. The model is essentially the same as that described in Fig. 4.27. Instead of a two-state model, we allow a continuous range of variation, 0 < > 2it. Also, and can be either negative or zero for a carboxylate or an amine group, respectively.

It was originally thought that one should be able to remove the succinic acid group by treatment of 7 with hydrazine in the same way one is able to produce a primary amine by treating a phthalimide with hydrazine in the classical Gabriel synthesis (12). This was not the case, though, since 7 did not react with hydrazine. However, it was found that treatment of 7 with dilute sodium hydroxide readily hydrolyzed the succinimide to produce the amino alcohol, 1, in 90% yield and having a 98 - 99% ee. 

In this transamination, the effect of para substitient groups has been studied using fluorinated phenylpyruvic acids and L-aspartic acid. From these results, the migratory preference is H > F > Cl > Br > CF3. This order has been attributed to the bulkiness of the substituted group [57]. Direct amination of p-substituted succinic acid with phenylalanine ammonialyase (EC 4.3.1.5) has suggested very high substrate specificity that the order of reaction rate is m-F o-F P-p-F >CF3. 

BA BuE-PA BE-HET BE-HHPA BE-MA BE-PA BE-SA CA CHX DMA DMBA DY 062 GA HEB HHPA HMTA MA MTHPA NMA benzoic acid monobutylester of phthalic acid monobenzylester of hexachloroendomethylenetetrahydrophthalic acid monobenzylester of hexahydrophthalic acid monobenzylester of maleic acid monobenzylester of phthalic acid monobenzylester of succinic acid citraconic anhydride cyclohexanol N,N-dimethylaniline dimethylbenzylamine high boiling tertiary amine (Ciba Geigy AG) gjptaric anhydride 2-hydroxy-4-(2,3-epoxypropoxy)benzophenone hexahydrophthalic anhydride hexamethylenetetramine maleic anhydride methyltetrahydrophthalic anhydride nadic methyl anhydride (methylbicyclo[2.2.1]heptene-2,3-dicarboxylic anhydride isomers)... 

Glyco-coated dendrimers possess a core structure of varied chemical nature, with a number of peripheral groups to which carbohydrate moieties are attached. The most common core structures are based on polyaminoamides (PAMAM) or poly(propyleneimine) (Astramol ) with a primary amine at the periphery, and these are commercially available. Polyamides based on N,N-bis(3-aminopropyl)glycine and A,Ar-bis(3-aminopropyl)succinic acid have also been prepared.78... 

Furandicarboxylic acid Fructose, glucose (via HMF intermediate) Diol, amine, levulinic acid, succinic acid, 2,5 -fu rand icarbaldehyde, 2,5-dihydroxymethyl-furan, tetrahydrofuran, polyethylene, terephthalate analogues. Werpy and Petersen 2004... 

Four main types of antioxidants are commonly used in polypropylene stabilizer systems although many other types of chemical compounds have been suggested. These types include hindered phenolics, thiodi-propionate esters, aryl phosphites, and ultraviolet absorbers such as the hydroxybenzophenones and benzotriazoles. Other chemicals which have been reported include aromatic amines such as p-phenylenediamine, hydrocarbon borates, aminophenols, Zn and other metal dithiocarbamates, thiophosphates, and thiophosphites, mercaptals, chromium salt complexes, tin-sulfur compounds, triazoles, silicone polymers, carbon black, nickel phenolates, thiurams, oxamides, metal stearates, Cu, Zn, Cd, and Pb salts of benzimidazoles, succinic acid anhydride, and others. The polymeric phenolic phosphites described here are another type. 

Combination of the reagents TiCU, BuaN, and TMSOTf, was reported to be effective for Claisen condensation, as exemplified in Eqs (42) and (43) [129]. When acyl-oxazolidinones were subjected to reaction with TiCU and a tertiary amine, homocoupling reaction at the a-position of the acyl group took place to give succinic acid derivatives [146], The lithium enolate of an ester or amide has been alkylated with an (N,C>)-acetal in the presence of Ti(0-/-Pr)4 (Eq. 44) [147,148]. 

Not unexpectedly, marine crankcase oils are sometimes contaminated with water, which is normally removed by the lubricating oil centrifuge. To assist further in protecting against rusting, inhibitors such as alkyl sulphonates, phosphonates, amines and alkyl succinic acids/esters can be added. They work by forming a hydrophobic film on the metal surface but must be selected with due regard to the other additives present. 

U.S. 4,486,338 (1984) Ootani et al. (Kao) Succinic acid derivative with anionic and tertiary amine oxide Superior foaming, detergency, and stability... 

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