Ritter

METHOD 4 This here method was contributed by a scholar named Ritter. She is adamant about this method and considers it a major breakthrough. Ritter wants to do what was done in Method 2 except without the insidious methylamine. 

Who Needs Methylamine Anyway by Ritter, edited by The Professor... 

Nitroethane and 1-(3,4 methylenedioxy) 2- nitropropane This method of producing the above mentioned nitro compounds is by far the best Ritter has come across yet The problem with standard nitroethane synthesis is that the -NO2 source most commonly used is silver nitrite (a la Merck Index citing). Needless to say, this is going to be an expensive compound to make as it is not available commercially but must be synthesized from costly silver nitrate. The other methods mentioned in Vogels 5th masterpiece... 

The last recipe deserves to be last The Ritter Reaction [not affiliated with the above Ritter]. 

This method was designed to produce an acetyl intermediate just like that in the failed recipe a few paragraphs above using only sulfuric acid and acetonitrile [93]. This reaction works, in theory, in a so-so manner on allylbenzene but not on safrole. This method will not make X for many reasons. So why does underground literature and DEA forensic scientists keep claiming that it does Strike doesn t know either. Let s see what the man who invented this. Dr. Ritter, had to say back in 1952 "several attempts to obtain amides from...safrol (sic) were fruitless. [94]. What makes all these people think that this will work unless no one did their homework. This is another sore spot of Strike s and... 

This next method was included with a submission by Ritter that appeared in the Theoretical section of this book. 

The technique of mercury porosimetry consists essentially in measuring the extent of mercury penetration into an evacuated solid as a function of the applied hydrostatic pressure. The full scope of the method first became apparent in 1945 when Ritter and Drake developed a technique for ... 

In their original work Drake and Ritter found that the curves of volume against pressure for the penetration and withdrawal did not coincide. Numerous investigations since then have confirmed that hysteresis is a general feature of mercury porosimetry. 

Method 4. Ritter reaction reaction of hydrogen cyanide with an olefin in an acidic medium to produce a primary amine. 

Ritter Reaction (Method 4). A small but important class of amines are manufactured by the Ritter reaction. These are the amines in which the nitrogen atom is adjacent to a tertiary alkyl group. In the Ritter reaction a substituted olefin such as isobutylene reacts with hydrogen cyanide under acidic conditions (12). The resulting formamide is then hydroly2ed to the parent primary amine. Typically sulfuric acid is used in this transformation of an olefin to an amine. Stoichiometric quantities of sulfate salts are produced along with the desired amine. 

CH3)2CH0H + CH2=C=0 CH3C00CH(CH3)2 and the Ritter reaction to prepare A/-isopropylacrylamide [2210-25-5] from acrylonitrile [107-13-1] and isopropyl alcohol ... 

Management Practices—U.S. Companies Improve Peformance Through Quality Efforts, United States General Accounting Office Report to the Honorable D. Ritter, House of Representatives, Washington, D.C., May 1991, p. 2. 

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