Organic Syntheses, Coll. Vol. 6, p.289 (1988); Vol. 53, p.86 (1973).
A 500-ml., four-necked, round-bottomed flask (Note 1)
equipped with a sealed mechanical stirrer (Note 2)
, a gas-inlet tube
, a low-temperature thermometer
, and a calcium chloride tube
is charged with 250 ml. of dry diethyl ether
. With an acetone–dry ice bath
the temperature of the ether
is lowered to −10 to −15° and maintained within this range while a slow stream (Note 3)
of hydrogen chloride
is introduced, with slow stirring, for about 45 minutes. The gas-inlet tube is replaced with a glass stopper
, and 10.0 g. (0.0259 mole) of cholestan-3-one (Note 4)
is added while the temperature of the stirred solution (Note 5)
is kept below −15°. The reaction mixture is cooled to −20°, and 12.3 g. (0.188 g.-atom) of activated zinc (Note 6)
is added over a 2–3 minute period. The temperature of the reaction mixture is allowed to rise to −5° (Note 7)
, and it is maintained between −4° and 0° (Note 8)
for 2 hours. Stirring is not interrupted for the duration of the reaction. The mixture is finally cooled to −15° and poured slowly onto about 130 g. of crushed ice. The ethereal layer is separated, and the aqueous layer is extracted with 100 ml. of ether
that had been used to rinse the reaction vessel. The ethereal solutions are combined, washed with saturated aqueous sodium chloride
, dried over anhydrous magnesium sulfate
, and filtered. The ether is distilled under reduced pressure with a 50° water bath
, leaving 9.3–9.5 g.
of a colorless, liquid residue that solidifies on cooling. This solid is dissolved in 30–40 ml. of n-hexane (Note 9)
. The solution is poured onto a 3.5 cm. by 17 cm. column
of silica gel (Note 10)
and eluted with 80–90 ml. of n-hexane
. Distillation of the solvent under reduced pressure with a 50° water bath leaves 8.0–8.2 g.
) of cholestane (Note 11)
, which, after recrystallization from ethanol-ether (Note 12)
, yields 7.3–7.5 g.
) of product as plates m.p. 78–79°
(lit., m.p. 80°
)3 (Note 13)
A standard, three-necked flask
fitted with a Y-tube
may be used.
An efficient magnetic stirrer
may be substituted.
Approximately one bubble per second can be spot-checked periodically by connecting the calcium chloride tube to an oil-filled bubble counter.
does not dissolve completely at this low temperature, but the reaction is not affected.
The submitters prepared activated zinc
by the following procedure. Commercial zinc powder (16 g.), special grade, ca. 300 mesh, obtained from either Kishida Chemical Company Ltd. or Hayashi Pure Chemical Company Ltd.
, is added with stirring to a 300-ml., round-bottomed flask
containing 100 ml. of 2% hydrochloric acid
. Vigorous stirring is continued until the surface of the zinc
becomes bright (ca.
4 minutes). The aqueous solution is decanted, and the zinc
powder in the flask is washed by decantation with four 200-ml. portions of distilled water. The activated zinc
powder is transferred to a suction filter
with 200 ml. of distilled water and washed successively with 50 ml. of ethanol
, 100 ml. of acetone
, and 50 ml. of dry ether
. Filtration and washing should be done as rapidly as possible to minimize exposure of the activated zinc
to air. The zinc
is finally dried at 85–90° for 10 minutes in a vacuum oven
15 mm.), cooled, and used immediately; the yield is 13–14 g.
The checkers used this procedure with certified zinc powder, 325 mesh, obtained from Fisher Scientific Company
This requires ca.
The temperature is regulated by adding pieces of dry ice to the cooling bath as required. As the reduction proceeds, the solution separates into two phases.
The solution is decanted from any insoluble matter.
Silicic acid, 100 mesh (Mallinckrodt)
, was used.
This material melts at 78–79°
. On TLC [silica, development with n-hexane
, visualization with sulfuric acid-methanol
(1:1) and heating] the product had Rf
= 0.74. An impurity, Rf
= 0.65, was present.
is dissolved in 50 ml. of ether
is distilled until the volume is 25 ml., 200 ml. of ethanol
is added, and the mixture is refrigerated.
Recovery is 92%
. Recrystallization has no effect on the quality of the product as judged by m.p. and TLC (Note 11)
The well-known Clemmensen reduction4
is a general method by which aralkyl ketones are readily converted to the corresponding hydrocarbons with amalgamated zinc
and hydrochloric acid
. It is not particularly effective, however, with alicyclic and aliphatic ketones. The procedure described herein provides a simple method of reducing a variety of ketones to their desoxy derivatives in high yields under much milder conditions (0°, 1–2 hours) than those normally used in the Clemmensen reaction.4
This permits selective deoxygenation of ketones in polyfunctional molecules5
containing groups such as cyano, amido, acetoxy
, and carboalkoxy, which are stable under the mild reaction conditions. For example, the following reduction6
has been carried out successfully by the modification of our procedure, using acetic anhydride
as the solvent.5
Wide latitude is permitted in choosing the solvent for the reaction. Several organic solvents (tetrahydrofuran
and particularly acetic anhydride5,8
may be used instead of dry ether. α-Halo- and α-acetoxycholestanone5
are converted to cholestane
O and also with Zn-HCl-Ac2
These reduction systems, however, have given different results with α,β-unsaturated ketones.9
yield, while cholest-4-en-3-one
gave an 88% yield of a mixture of 1.2 parts of cholestane
and 1 part of coprostane
. By contrast, reaction of Zn-HCl-Ac2
O with cholest-1-en-3-one
afforded a mixture of three compounds: cholestane
), and cholestan-3-one
appears to be formed from the corresponding cyclopropanol acetate10
during the work up. The mechanism of this reduction is probably similar to that of the Clemmensen reaction.11
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