Download Document

12-7 Oxymercuration-Demercuration: A Special
Electrophilic Addition
The electrophilic addition of a mercuric salt to an alkene is called mercuration.
The product formed is known as an alkylmercury derivative.
A reaction sequence known as “oxymercuration-demercuration” is a useful
alternative to acid-catalyzed hydration:
Oxymercuration is anti stereospecific and regioselective.
The alcohol obtained from oxymercuration-demercuration is the same as that
obtained from Markovnikov hydration, however, since no carbocation is involved
in the reaction mechanism, rearrangements of the transition state do not occur.
Oxymercuration-demercuration in an alcohol solvent yields an ether:
12-8 Hydroboration-Oxidation: A Stereospecific Anti-
Markovnikov Hydration
The boron-hydrogen bond adds across double bonds.
Borane, BH3, adds to double bonds without catalytic activation:
The borane is commercially
available in an ethertetrahydrofuran solvent.
Hydroboration is regioselective as well as stereospecific (syn addition).
Here, steric factors are more important than electronic factors. The boron binds
to the less hindered (substituted) carbon.
The oxidation of alkylboranes gives alcohols.
The oxidation of a trialkylborane by hydrogen peroxide produces an alcohol in
which the hydroxyl group has replaced the boron atom.
In this reaction, the hydroxyl group ends up at the less substituted carbon: an antiMarkovnikov addition.
12-9 Diazomethane, Carbenes and Cyclopropane
Synthesis
Cyclopropanes can be readily prepared by the addition of a carbene to the double
bond of an alkene.
A carbene has the general structure, R2C:, in which the central carbon is
surrounded by six electrons (sextet), and is thus electron deficient.
The electron-deficient carbene readily adds to an electron rich alkene.
Diazomethane forms methylene, which converts alkenes into
cyclopropanes.
The highly reactive species methylene, H2C: (the simplest carbene) can be
produced from the decomposition of diazomethane:
When methylene is generated in the presence of an alkene, an addition reaction
occurs producing a cyclopropane. This reaction is usually stereospecific, with
retention of the original double bond configuration.
Halogenated carbenes and carbenoids also give cyclepropanes.
Halogenated carbenes, prepared from halomethanes, can also be used to
synthesize cyclopropanes.
Treatment of trichloromethane (chloroform) with strong base causes an
elimination reaction in which both a proton and a chlorine atom are removed
from the same carbon.
The resulting product is a dichlorocarbene which reacts with alkenes to produce
cyclopropanes.
To avoid the hazards associated with diazomethane preparation, an alternate
route using diiodomethane and zinc (Simmons-Smith reagent) to produce ICH2ZnI
is used.
This substance is an example of a carbenoid, a carbenelike substance that
converts alkenes into cyclopropanes stereospecifically.