The aqueous layer was extracted with ethyl acetate (2 20 mL the combined organic layers were washed with water (2 20 mL dried over sodium sulfate and evaporated under vacuum.
"Reductive amination of oxygen-containing organic compounds".
Employing a ketone will result in a branched alkyl substituent on the amine.Each of these NC bonds could potentially be formed through reductive amination, since they have C-H bonds.1,2-Dichloroethane (DCE) is the preferred reaction solvent, but reactions can also be carried out in tetrahydrofuran and occasionally in acetonitrile.Reductive Amination, enter reductive amination!N -Allylbenzylamine (1f) 1H NMR (300 MHz, CDCl3).387.08 (m,.89 (ddt,.2,.4,.1 Hz,.215.10 (m,.74 (s,.21 (d,.1 Hz,.00 (bs, 1H 13C NMR (75.4 MHz, CDCl3) 139.6, 136.2, 128.6, 128.1, 127.2, 116.8.If the file has been modified from its original state, some details such as the timestamp may not fully reflect those of the original file.9 In industry, tertiary amines such as triethylamine and diisopropylethylamine are formed directly from ketones with a gaseous mixture of ammonia and hydrogen and a suitable catalyst.
That means that there are three possible ways of making this amine through reductive amination, all of them acceptable!
Methyl iodide, CH3I ) idée cadeau 300 euros will result in significant formation of the undesired tertiary amine (i.e.
Ketones Also Work, what about ketones?An even better approach involves the use of the slightly weaker reducing agent sodium cyanoborohydride (NaBH3CN).Share alike, if you alter, transform, or build upon this work, you may distribute the resulting work only under the same or similar license to this one.Reductive amination (also known as reductive alkylation ) is a form of amination that involves the conversion of a carbonyl group to an amine via an intermediate imine.Sodium triacetoxyborohydride is a general, mild, and selective reducing agent for the reductive amination of various aldehydes and ketones.See article for more examples, key Words, reductive Amination, Amines, Aldehydes, Ketones, Sodium triacetoxyborohydride, Sodium borohydride.Buchwald-Hartwig cross coupling is one of them.Reduce the imine with a reductant such as sodium cyanoborohydride (NaBH3CN sodium borohydride (NaBH4 or sodium tri-acetoxyborohydride (NaBH(OAc)3) giving promo peugeot 208 essence a new amine.



(Note that reductive amination doesnt work for installing a phenyl group. .
At mildly acidic pH, the carbonyl oxygen is protonated, speeding up the rate of addition to the carbonyl carbon; if the solution is too acidic, however, the amine nucleophile will be converted into its (non-nucleophilic) conjugate acid, an ammonium salt, and no reaction will occur.

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