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Most common imides are prepared by heating dicarboxylic acids or their anhydrides and ammonia or primary amines. The result is a condensation reaction: [5] (RCO) 2 O + R′NH 2 → (RCO) 2 NR′ + H 2 O. These reactions proceed via the intermediacy of amides. The intramolecular reaction of a carboxylic acid with an amide is far faster than the ...
Treatment of the resulting compound with ammonia then completes the conversion to the amidine. [1] Instead of using a Bronsted acid, Lewis acids such as aluminium trichloride promote the direct amination of nitriles, [2] or, in certain exceptional cases, of amides. [3] Dimethylformamide acetal reacts with primary amines to give amidines: [4]
The general structure of an imine. In organic chemistry, an imine (/ ɪ ˈ m iː n / or / ˈ ɪ m ɪ n /) is a functional group or organic compound containing a carbon–nitrogen double bond (C=N). The nitrogen atom can be attached to a hydrogen or an organic group (R). The carbon atom has two additional single bonds.
The Forster–Decker method is a series of chemical reactions that have the effect of mono-alkylating a primary amine (1), forming a secondary amine (6). [ 1 ] [ 2 ] The process occurs by way of transient formation of an imine ( 3 ) that undergoes the actual alkylation reaction.
Amidoximes are oximes of amides (R 1 C(=O)NR 2 R 3) with general structure R 1 C(=NOH)NR 2 R 3. Oximes are usually generated by the reaction of hydroxylamine with aldehydes (R−CH=O) or ketones (RR’C=O). The term oxime dates back to the 19th century, a combination of the words oxygen and imine. [1]
The Eschweiler–Clarke reaction (also called the Eschweiler–Clarke methylation) is a chemical reaction whereby a primary (or secondary) amine is methylated using excess formic acid and formaldehyde. [1] [2] Reductive amination reactions such as this one will not produce quaternary ammonium salts, but instead will stop at the tertiary amine ...
In organic chemistry, a hemiaminal (also carbinolamine) is a functional group or type of chemical compound that has a hydroxyl group and an amine attached to the same carbon atom: −C(OH)(NR 2)−. R can be hydrogen or an alkyl group. Hemiaminals are intermediates in imine formation from an amine and a carbonyl by alkylimino-de-oxo ...
This reaction is believed to occur in three steps. First, the amine is oxidized to the corresponding imine, with reduction of the FAD cofactor to FADH 2. Second, O 2 accepts two electrons and two protons from FADH 2, forming H 2 O 2 and regenerating FAD. Third, the imine is hydrolyzed by water, forming ammonia and the aldehyde. [7] [8]