Organic Syntheses, Coll. Vol. 4, p.221 (1963); Vol. 34, p.19 (1954).
[I. NITROUS ACID METHOD]
A solution of sodium ethoxide is prepared by adding 57.5 g. (2.5 g. atoms) of clean sodium to 1.2 l. of absolute ethanol (Note 2)
in a 3-l. three-necked flask equipped with an Allihn reflux condenser fitted with a drying tube, a large sturdy sealed Hershberg stirrer, and a dropping funnel
. After the sodium
has dissolved, the solution is cooled to 40° and the condenser is replaced by a thermometer
extending into the liquid. A mixture of 245.5 g. (258.5 ml., 2.5 moles) of redistilled cyclohexanone
and 198 g. (175 ml., 3.25 moles) of redistilled nitromethane (Note 3)
is added dropwise with vigorous stirring over the course of about 3 hours at a rate that maintains an internal temperature of 45 ± 3° (Note 4)
. After addition is complete, the white, pasty mass is stirred for an additional 3 hours without cooling or heating and then is allowed to stand overnight. The resulting suspension is cooled with an ice bath
, and the white sodium salt of 1-(nitromethyl)cyclohexanol
is collected on a 25-cm. Büchner funnel
and dried by suction for about 1 hour (Note 1)
. The sodium salt cake is broken up and transferred to a 4-l. beaker equipped with a Hershberg stirrer and immersed in an ice bath
. A cold solution of 184 g. (175 ml., 3 moles) of glacial acetic acid
in 1250 ml. of water is added in a single portion, and the mixture is stirred for 10–30 minutes to complete dissolution. The oily layer of 1-(nitromethyl)cyclohexanol
is separated, and the aqueous layer is extracted with three 100-ml. portions of ether
. The ether
extracts and the 1-(nitromethyl)cyclohexanol
are combined, dried briefly over magnesium sulfate
, and concentrated by distillation from a steam bath
with a water aspirator
at 20–35 mm. to remove ether
and excess nitromethane
. The crude, undistilled 1-(nitromethyl)cyclohexanol (Note 5)
is dissolved in 450 ml. of glacial acetic acid
in a 2-l. externally cooled stainless-steel hydrogenation bottle (Note 6)
. Three heaping teaspoonfuls of W-4 Raney nickel catalyst2
are added, and the mixture is shaken with hydrogen
at 40–45 p.s.i., with cooling to maintain the temperature below 35°, until about 90%
of the theoretical amount (7.5 moles
) is taken up and absorption ceases (Note 7)
. The catalyst is separated by filtration with suction through Filter-Cel, and the filtrate (sometimes green or tan) containing the 1-(aminomethyl)cyclohexanol
is used directly in the next step (Note 8)
The filtrate is transferred to a 5-l. round-bottomed flask, immersed in an ice-salt mixture and equipped with a Hershberg stirrer, a thermometer, and a dropping funnel
. The solution is diluted with 2.3 l. of ice water; then an ice-cold solution of 290 g. (4.2 moles) of sodium nitrite
in 750 ml. of water is added dropwise during a period of about 1 hour with stirring and cooling (ice-salt bath
) to maintain the temperature at −5°. The mixture is stirred for an additional period of 1 hour and then allowed to come to room temperature overnight as the ice in the cooling bath melts. The acetic acid
in the reaction mixture is neutralized by the addition of small portions of solid sodium bicarbonate
, and the neutral (to litmus paper) solution is then steam-distilled until about 2 l. of distillate is collected. The oily cycloheptanone
layer is separated, the aqueous layer is extracted with three 100-ml. portions of ether
, and the combined organic layers are dried briefly over magnesium sulfate
. Most of the ether
is removed by distillation through a 17 by 2.5 cm. glass helix-packed column
at atmospheric pressure (Note 9)
. The residue is then distilled through the same column, and the fraction boiling at 80–85°/30 mm.
is collected. The yield of cycloheptanone
is 112–118 g.
1.4600 (Note 10)
and (Note 11)
It has been reported3
that when the crude product from the condensation of 2 moles of nitromethane
(as the sodium salt in absolute ethanol
) with 1 mole of 1,1,3,3-tetramethylcyclobutane-2,4-dione (dimethylketene dimer)
was filtered, and the filter cake was dried on a porous clay plate, a violent explosion occurred upon addition of the dried powder to crushed ice.
This experience suggests that it may be inadvisable to dry completely the sodium salt of 1-(nitromethyl)cyclohexanol
, and that the material should be handled with considerable caution. Also, in other procedures where salts of nitro compounds are involved, and the extent of the reaction and the nature of the products are not known with certainty, the salts probably should not be filtered, but should be neutralized in the reaction mixtures and the free nitro alcohols separated by suitable means.
Commercial absolute ethanol
is used without additional drying. The submitters state that the use of absolute ethanol
may be avoided by employment of the alternative condensation procedure of Wood and Cadorin4
using 5 mole per cent of sodium hydroxide in aqueous methanol
at 15–20° for 6 hours, but the yield of 1-(nitromethyl)cyclohexanol
is appreciably lower (51%
is dried over magnesium sulfate
or calcium sulfate (Drierite)
for 1 day and distilled; the fraction boiling at 152.5–154°
(uncor.) is used. Nitromethane
is dried in the same manner and distilled; small quantities of acidic impurities are removed in the fore-run, and the fraction boiling at 101.5–102.5°
(uncor.) is used. Drying is frequently unnecessary when good grades of cyclohexanone and nitromethane
Efficient stirring of the pasty reaction mixture is necessary to obtain maximum yield.
Removal of residual amounts of acetic acid
in the crude product is unnecessary; their presence is actually preferable to the presence of traces of bases, such as any sodium bicarbonate
remaining from neutralization, which reverse the condensation on attempted distillation of 1-(nitromethyl)cyclohexanol
The submitters state that, in preparations conducted on twice the scale specified, fractional distillation of the residue yielded 620–670 g.
) of 1-(nitromethyl)cyclohexanol
, b.p. 129–132°/19 mm.
A Pyrex bottle
can be used; it must be enclosed to prevent possible injury by fragments of glass in case of explosion.
Catalytic hydrogenation of 1-(nitromethyl)cyclohexanol
in acetic acid
solvent is a markedly exothermic reaction, and, unless the temperature is moderated to about 35°, low yields of 1-(aminomethyl)cyclohexanol
result owing to hydrogenolysis and deactivation of the catalyst. Cooling can be accomplished by running cold water through a copper coil surrounding the hydrogenation bottle or by periodically adding ice to the container in which the bottle is placed. Considerable cooling is necessary during initial stages of the hydrogenation, but cooling below 25° greatly retards the reduction. Absorption of hydrogen
is usually complete in 15–18 hours under these conditions, but longer times may be required, depending on the temperature and pressure and on the amount and activity of the catalyst.
can be isolated as its acetic acid salt by the addition of 2 volumes of ether
to the acetic acid
solution or to the residue after removal of the acetic acid
under reduced pressure, followed by trituration and refrigeration overnight. After filtration of the first crop of crystals, m.p. 118–121°
, a second crop of the salt, m.p. 113–116°
, is obtained on removal of the dissolved nickel
from an aqueous solution of the concentrated filtrate by saturation with hydrogen sulfide
, concentration, and treatment with ether
. Total yields of the air-dried crude acetic acid salt of 1-(aminomethyl)cyclohexanol
obtained from 100–350 g. lots of 1-(nitromethyl)cyclohexanol
in this manner ranged from 69% to 94%.
Distillation of the product from a modified Claisen flask
and collection of the fraction boiling at 67–77°/20 mm. (largely 69–72°)
gave 140–149 g.
of impure cycloheptanone
1.4570–1.4590, containing about equal amounts (10–15 g.) of lower-boiling and higher-boiling (mainly 1-(nitromethyl)cyclohexanol)
contaminants, which were separated by distillation through the glass helix-packed column
The submitters state that the yields of cycloheptanone
obtained from 60- to 700-g.
quantities of the crude acetic acid salt of 1-(aminomethyl)cyclohexanol
(isolated by the procedure of ((Note 8)
) were 57–65%.
[II. DIAZOMETHANE METHOD]
is very toxic; therefore the operations must be carried out in a well-ventilated hood
. (See p. 250
In a 500-ml. round-bottomed flask, provided with a mechanical stirrer (Note 1)
, a thermometer
, and a dropping funnel
, are placed 49 g. (0.5 mole) of cyclohexanone (Note 2)
, 125 g. (0.58 mole) of p-tolylsulfonylmethylnitrosamide (p. 943)
, 150 ml. of 95% ethanol
, and 10 ml. of water (Note 3)
. The nitroso compound is largely undissolved. The stirrer is adjusted so that only the upper portion of solution is stirred and the precipitate moves slightly. The thermometer
bulb is placed in the liquid.
The reaction mixture is cooled to about 0° with an ice-salt bath; then with gentle stirring a solution of 15 g. of potassium hydroxide
in 50 ml. of 50% aqueous ethanol
is added dropwise very slowly from the dropping funnel. After the addition of 0.5–1 ml. of the alkaline solution a brisk evolution of nitrogen
commences and the temperature rises. The rate of addition is adjusted so that the temperature is maintained at 10–20° (Note 4)
. The addition of the alkali requires about 2 hours, during which the nitroso compound gradually disappears. The orange-yellow solution is stirred for an additional 30 minutes, then 2N hydrochloric acid (about 50 ml.)
is added until the solution is acidic to litmus paper.
A solution of 100 g. of sodium bisulfite (Note 5)
in 200 ml. of water is added as stirring is continued. After a few minutes a thick precipitate separates. The mixture is stirred or preferably shaken mechanically at room temperature with exclusion of air for 10 hours. The bisulfite addition product is separated by suction filtration, washed with ether
until colorless, and decomposed in a flask with a lukewarm solution of 125 g. of sodium carbonate
in 150 ml. of water. The ketone layer is separated, the aqueous layer is extracted with four 25-ml. portions of ether
, and the combined organic layers are dried over anhydrous sodium sulfate
. Most of the ether
is removed by distillation at atmospheric pressure, and the residual oil is distilled at reduced pressure (Note 6)
After a few drops of fore-run, practically all the liquid distils at 64–65°/12 mm.
The yield of cycloheptanone
is 18.5–20.2 g.
) (Note 6)
If it is desired to determine the amount of nitrogen
evolved, then it is necessary to use a sealed stirrer and a discharge tube for the nitrogen
; however, observing the amount of nitrogen
evolved affords no particular advantage. The temperature exerts sufficient control on the reaction rate, and dissolution of the nitroso compound indicates the progress of the reaction.
In some experiments, the temperature was allowed to rise temporarily to 35° without mishap, but the lower temperature is preferred for reasons of safety.
, which is a by-product, is removed at this stage since it does not form an adduct with bisulfite.
The checkers found it desirable to distil the product through a fractionating column
in order to effectively remove the small fore-run and a smaller after-run. The pattern obtained in a 50-cm. column of the simple Podbielniak type
follows: fraction 1, 1.13 g., b.p. up to 63°/12 mm.
1.4549; fraction 2, 19.44 g., b.p. 63–64°/12 mm.
1.4592; fraction 3, 0.55 g., b.p. > 64°/12 mm.
1.4604. A center cut of fraction 2 had n25D
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