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1-Aminopentane is an organic compound with the formula CH 3 (CH 2) 4 NH 2. It is used as a solvent , as a raw material in the manufacture of a variety of other compounds, including dyes, emulsifiers , and pharmaceutical products, [ 1 ] and as a flavoring agent .
A concentrated solution of sodium chloride in water, known as a brine solution, is added to the mixture and the layers are allowed to separate. The brine is used to remove any acid or water from the organic layer. In this example the organic layer is the product, which is a liquid at room temperature.
HATU is commonly encountered in amine acylation reactions (i.e., amide formation). Such reactions are typically performed in two distinct reaction steps: (1) reaction of a carboxylic acid with HATU to form the OAt-active ester; then (2) addition of the nucleophile (amine) to the active ester solution to afford the acylated product.
[2] The intermediate imine can be isolated or reacted in-situ with a suitable reducing agent (e.g., sodium borohydride) to produce the amine product. [2] Intramolecular reductive amination can also occur to afford a cyclic amine product if the amine and carbonyl are on the same molecule of starting material. [4]
The amine is condensed with the carbonyl followed by addition of the boronic acid . [1] Alpha amino acid synthesis. One of the most attractive features of the Petasis reaction is the stability of the vinyl boronic acids. With the advent of the Suzuki coupling, many are commercially available. organoboronic acid synthesis
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Aminopentane may refer to: 1-Aminopentane; 2-Aminopentane; 3-Aminopentane This page was last edited on 4 August 2019, at 16:05 (UTC). Text is available under the ...
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