- In
organic chemistry, the
Menshutkin reaction converts a
tertiary amine into a
quaternary ammonium salt by
reaction with an
alkyl halide.
Similar reactions...
- and nature.
Menshutkin 1952, p. 15.
Menshutkin 1952, p. 16.
Menshutkin 1952, p. 20.
Menshutkin 1952, p. 17.
Menshutkin 1952, p. 23.
Menshutkin 1952, p. 24...
-
Nikolai Aleksandrovich Menshutkin (Russian: Николай Александрович Меншуткин; 24
October [O.S. 12 October] 1842 – 5 February [O.S. 22 January] 1907) was...
-
Hydroamination is
another green method for N-alkylation.[citation needed] In the
Menshutkin reaction, a
tertiary amine is
converted into a
quaternary ammonium salt...
-
tertiary amines by
alkyl halides. This is
often hampered by an
unwanted Menshutkin reaction forming a
quaternary ammonium salt, but is
absent when DIPEA...
-
Graebe (discoverer of alizarin),
Oscar Loew,
Constantin Fahlberg,
Nikolai Menshutkin,
Vladimir Markovnikov (first to
describe carbocycles smaller and larger...
-
tertiary amine the
reaction product is a
quaternary ammonium salt in the
Menshutkin reaction: R 3 − N | R 2 R 1 | : ⏟
tertiary amine + R 4 X ⏟ halogeno- alkane...
-
react with DCM to form
quaternary chloromethyl chloride salts via the
Menshutkin reaction.
Secondary amines can
react with DCM to
yield an equilibrium...
- is
typically combined with the rest of the
surfactant molecule via a
Menshutkin reaction with a
tertiary amine.
Hydroxysultaines are also
compatible with...
-
halides is
widely do****ented. In
older literature this is
often called a
Menshutkin reaction,
however modern chemists usually refer to it
simply as quaternization...
