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The Beckmann Rearrangement. The archetypal Beckmann rearrangement [4] is the conversion of cyclohexanone to caprolactam via the oxime. Caprolactam is the feedstock in the production of Nylon 6. [5] The Beckmann solution consists of acetic acid, hydrochloric acid and acetic anhydride, and was widely used to
The most famous and commercially important reaction of cyclohexanone oxime is Beckmann rearrangement yielding ε-caprolactam, which is used to produce Nylon 6: This reaction is catalyzed by sulfuric acid, [1] but industrial scale reactions use solid acids. [2] Typical of oximes, the compound can be reduced by sodium amalgam to produce ...
About half of the world's supply of cyclohexanone, more than a million tonnes annually, is converted to the oxime. In the presence of sulfuric acid catalyst , the oxime undergoes the Beckmann rearrangement to give the cyclic amide caprolactam: [ 19 ]
It was estimated that 90% of all caprolactam is synthesised from cyclohexanone (1), which is first converted to its oxime (2). Treatment of this oxime with acid induces the Beckmann rearrangement to give caprolactam (3): [2] The immediate product of the acid-induced rearrangement is the bisulfate salt of caprolactam.
It has been estimated that 90% of all caprolactam is synthesised from cyclohexanone (1), which is first converted to its oxime. Treatment of this oxime with acid induces the Beckmann rearrangement to give caprolactam: [8] The Beckmann rearrangement has also been used for the introduction of nitrogen into codeine. [9]
Conversion of cyclohexanone to caprolactam involving the Beckmann rearrangement. Approximately 95% of hydroxylamine is used in the synthesis of cyclohexanone oxime, a precursor to Nylon 6. [11] The treatment of this oxime with acid induces the Beckmann rearrangement to give caprolactam. [21]
The time needed to connect power-hungry data centres to the electricity grid could blunt France's advantage using its abundant nuclear power to lure billions of dollars of investment into ...
2.1 Beckmann rearrangement. 2.2 Schmidt reaction. 2.3 Cyclization of amino acids. 2.4 Intramolecular nucleophilic substitution. ... Cyclohexanone with hydrazoic acid, ...