Org. Synth. 1955, 35, 62
DOI: 10.15227/orgsyn.035.0062
ETHYL ISOCYANIDE
Submitted by H. L. Jackson and B. C. McKusick
1.
Checked by N. J. Leonard and L. E. Coleman, Jr..
1. Procedure
Caution! This preparation should be carried out in a
well-ventilated hood because
ethyl isocyanide has a vile odor. Since
ethyl isocyanide has been known to explode,
2 all operations in which it is heated, including its distillation, should be carried out behind a shield of safety glass.
Silver cyanide (454 g., 3.40 moles) is added with stirring to 530 g. (3.40 moles) of ethyl iodide in a 3-l. three-necked round-bottomed flask, equipped with a reflux condenser and a sealed Hershberg stirrer. The third neck of the flask is closed with a stopper. The lower third of the flask is immersed in a steam bath, and the mixture is stirred vigorously until it turns to a viscous, homogeneous, brown liquid (1.7–2.3 hours). Stirring is interrupted, the steam bath is removed, and the stirrer is raised to a position just above the liquid (Note 1). Water (300 ml.) is added through the condenser to avoid loss of product during the addition. Potassium cyanide (610 g., 9.37 moles) and 260 ml. of water are then added through the third neck of the flask, and the mixture is stirred for about 10 minutes, during which the heavy brown liquid below the aqueous solution disappears and a brown layer of ethyl isocyanide appears above the aqueous solution. Stirring is discontinued, the reflux condenser is replaced by one arranged for distillation, and a thermometer extending into the aqueous layer is placed in the third neck. A receiver immersed in an ice bath is attached to the condenser, and the reaction mixture is heated by means of an electric heating mantle, causing a mixture of oil and water to distil. When the distillate contains almost no oil (Note 2), the distillation is discontinued (Note 3). The receiver contains about 200 ml. of crude ethyl isocyanide and 50 ml. of water. Sodium chloride (7 g.) is dissolved in the aqueous layer, and the ice-cold mixture is poured into a separatory funnel. The aqueous layer is separated and discarded. The ethyl isocyanide is washed with two 50-ml. portions of ice-cold saturated aqueous sodium chloride solution and is dried overnight with 10 g. of anhydrous magnesium sulfate. The decanted material is distilled through a 5- to 10-plate column (Note 4), giving 88–102 g. (47–55% yield) of ethyl isocyanide, b.p. 77–79°/760 mm., nD20 1.3632. The fore-run, b.p. 63–77°/760 mm., amounts to 15–46 g. and contains 10–15% of ethyl iodide and possibly a few drops of water. Additional pure ethyl isocyanide can be obtained by drying and redistilling this fore-run.
2. Notes
1.
Sometimes the liquid crystallizes to a dense solid which immobilizes the stirrer if it has not been raised. The crystallization has no effect on subsequent steps except to necessitate a longer period of stirring after the
potassium cyanide is added.
2.
The temperature of the residual mixture is 115–120° at this point.
3.
The aqueous cyanide solution, which is very toxic, can be disposed of by flushing it down the drain with a large volume of water.
4.
The submitters used an
18-in. spinning-band column (inside diameter 10 mm.). The checkers employed a
12-in. helix-packed column.
3. Discussion
Ethyl isocyanide has been obtained by treating
ethylamine and
chloroform with
potassium hydroxide,
3 by pyrolyzing the complex between
ethyl isothiocyanate and
triethylphosphine,
4 by heating
cyanocobaltic (III) acid with
ethanol,
5 by passing
ethylene and
hydrogen cyanide through an electric discharge,
6 or by heating
ethyl iodide with
silver cyanide7,8,9 or other metal cyanides.
8,10 The present procedure differs from earlier ones using
silver cyanide mainly in that a stirrer is employed. By this modification more than half of the
silver cyanide can be converted to
ethyl isocyanide, contrary to the belief of the earlier workers, who thought that this was precluded by formation of a complex, C
2H
5NC·AgCN.
This preparation is referenced from:
Appendix
Chemical Abstracts Nomenclature (Collective Index Number);
(Registry Number)
cyanocobaltic (III) acid
ethanol (64-17-5)
chloroform (67-66-3)
sodium chloride (7647-14-5)
hydrogen cyanide (74-90-8)
potassium cyanide (151-50-8)
potassium hydroxide (1310-58-3)
ethylene (9002-88-4)
magnesium sulfate (7487-88-9)
Ethyl iodide (75-03-6)
ethyl isothiocyanate (542-85-8)
silver cyanide (506-64-9)
Ethyl isocyanide (624-79-3)
ethylamine (75-04-7)
triethylphosphine (554-70-1)
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