PPA

Ethoxy carbonyl)-7-nitro Ethyl 2-niethyl-3-oxobutanoate PPA 78 [5]... 

One series of POD has been prepared from the corresponding dicarboxyhc acid/acid chlorides and hydra2ine sulfate in polyphosphoric acid (PPA) (50,51), one of the most common techniques for this type of backbone. 

Poly(l,3,4-oxadia2ole-2,5-diyl-vinylene) and poly(l,3,4-oxadia2ole-2,5-diyl-ethynylene) were synthesi2ed by polycondensation of fumaramide or acetylene-dicarboxamide with hydra2ine sulfate in PPA to study the effect of the two repeating units on polymer electronic and thermal properties (55). 

Possible tape materials include polyimide, polyester, polyethersulfone (PES), and polyparabanic acid (PPA) (18). Of these, polyimide is the most widely used material because its high melting point allows it to survive at temperatures up to 365°C. Although polyester is much cheaper than other materials, its use is limited to temperatures less than 160°C. PES and PPA, on the other hand, are half as cosdy as polyimide, and can survive maximum short-term temperatures of 220 and 275°C, respectively. PES has better dimensional stabiUty than polyimide, absorbs less moisture, and does not tear as easily however, it is inflammable and can be attacked by certain common solvents. Table 7 Hsts various plastic tapes and their properties. Common bump materials are gold, copper, and 95% Pb/5% Sn solder (see Tables 6 and 8 for properties see also References 2 and 21). 

Property Nylon-4,6 Nylon-MXD.6 Nylon-NDT/INDT Polyphthalamide (PPA)... 

A number of high melting poiat semiaromatic nylons, iatroduced ia the 1990s, have lower moisture absorption and iacreased stiffness and strength. Apart from nylon-6 /6,T (copolymer of 6 and 6,T), the exact stmcture of these is usually proprietary and they are identified by trade names. Examples iaclude Zytel HTN (Du Pont) Amodel, referred to as polyphthalamide or PPA (Amoco) and Aden (Mitsui Petrochemical). Properties for polyphthalamide are given ia Table 2. A polyphthalamide has been defined by ASTM as "a polyamide ia which the residues of terephthaUc acid or isophthahc acid or a combination of the two comprise at least 60 molar percent of the dicarboxyhc acid portion of the repeating stmctural units ia the polymer chain" (18). 

Fig. 13. The introduction of a modulator electrode in a Bayard-Alpert gauge permits the pressure range to be lowered by a factor of 10 to 133 pPa...

The only example of a simple pyridopyridazine synthesis of this kind from a pyridine intermediate involves a variant of a well known cinnoline synthesis in which the Japp-Klingemann intermediate (363) gives the pyrido[3,4-c]pyridazine (364) with PPA (69JHC977). 

Phenethyl carbamate derivatives 30 have also been employed in Bischler-Napieralski reactions cyclization of these substrates affords 3,4-dihydroisoquinolones 31. These reactions have been conducted using a variety of different promoters including PPA, POCl3, and Tf20. Mixtures of P2O5 and POCI3 appear to afford the best results in some cases. 

Many acids other than sulfuric acid have been used for the challenging cyclodehydration step. It is important to note that when the concentration of sulfuric acid is below 70%, hydrolysis of the imine or enamine occurs. As previously mentioned, HCl/AcOH, ZnCla, PPA, POCI3, and lactic acid have been successfully applied to promote the cyclization. Chloroacetic acid was found to perform similar to lactic acid. Concentrated HCl, p-TsOH, and have proven beneficial in generating linear... 

We have previously discussed that keto-aldehydes react with anilines first at the aldehyde carbon to form the aldimine. Subsequent condensation with another aniline formed a bis-imine or enamino-imine. The aniline of the ketimine normally cyclizes on the aldimine (24 —> 26). Conversely, cyclization of the aldimine could be forced with minimal aniline migration to the ketimine using PPA (30 —> 31). The use of unsymmetrical ketones has not been thoroughly explored a few examples are cited below. One-pot enamine formation and cyclization occurred when aniline 48 was reacted with dione 49 in the presence of catalytic p-TsOH and heat. Imine formation occurred at the less-hindered ketone, and cyclization with attack on the reactive carbonyl was preferred. ... 

Imine preparation from a tricarbonyl system followed by PPA promoted... 

Imine formation by reaction of aniline 58 and dione 49 under thermal conditions gave a mixture of imines. Cyclodehydration using PPA gave nearly a 1 1 mixture of isomers 59 and 60. These authors attempted thermal cyclization conditions (similar to Gould-Jacobs type conditions) to affect cyclization of this mixture and failed. Also, these authors reported difficulty in the clean formation of the imine. They observed large amounts of the A -acetyl compound presumably coming from fragmentation of the imine at the reported temperature... 

The cyclization step has been reported to work well in triglyme, mineral oil, paraffin, Dowtherm A , Ph20 or polyphosphoic acid (PPA). PPA has been used to promote the entire reaction in a single process (vide infra). 

More importantly, Peet and coworkers reported the reaction of o-nitroaniline 35 with acetylene dicarboxylate 32 to provide fumarate 36. Subsequent cyclization proved difficult under thermal conditions and only a 35% yield of quinolone 37 was isolated. Use of PPA for the cyclization improved the yield of 37 significantly. Using this modification allowed enamino-ester formation with a nitro-group attached to the arylamine. 

Reaction of 2-aininopyridine 59 with 3-keto-ester 60 in PPA provided pyrido-pyrimidine 61 in poor yield. Interestingly, upon heating isolated 61, rearrangement occurred to provide napthyridone 62 in good yield. 

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