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Selective monoalkylation of amines with light electrophiles using a flow microreactor system†
Thomas Lebleu,Jacques Maddaluno,Julien Legros
Organic Chemistry Frontiers Pub Date : 02/03/2015 00:00:00 , DOI:10.1039/C4QO00342J
Abstract

The challenging direct monoalkylation of amines with light electrophilic reagents (C1 to C3) was performed through a flow microreactor approach. The efficiency of mixing coupled with short residence times (tR = 0.7–62 s) allows the transfer of a single alkyl group from R-OTf onto primary amines (R = Et, Pr) as well as on secondary amines (R = Me, Et, Pr, allyl, propargyl) with good selectivities.

Graphical abstract: Selective monoalkylation of amines with light electrophiles using a flow microreactor system
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