Org. Synth. 1944, 24, 89
DOI: 10.15227/orgsyn.024.0089
SELENOPHENOL
[Benzeneselenol]
Submitted by Duncan G. Foster
Checked by C. F. H. Allen and H. W. J. Cressman.
1. Procedure
Most selenium compounds are toxic, and many have a vile odor. It is frequently advisable to work with them on alternate days. All manipulations should be done in a good hood. Rubber gloves should be worn, and it is well to keep the window of the hood down so that the glass is between the apparatus and the face of the operator.
Hydrogen selenide, a possible by-product, is very toxic, being comparable with hydrogen cyanide. Its accidental inhalation in small amounts may produce a sore throat.
A
500-ml. three-necked round-bottomed flask is fitted with an
efficient reflux condenser, a
glycerol-sealed mechanical stirrer, a
dropping funnel, and a
gas inlet tube extending nearly to the blades of the stirrer
(Note 1). An absorption train,
1 with the addition in
J of a safety tube which extends nearly to the bottom, is connected to the upper end of the reflux condenser
(Note 2). A 2-cm. layer of water in
J allows it to serve as a bubble counter;
K is one-third filled with a
50% potassium hydroxide solution. The entire apparatus is set up in subdued light in a hood and swept with dry
hydrogen (Note 3) and
(Note 4).
Phenylmagnesium bromide is prepared in the flask by the usual procedure
2 from
78.5 g. (0.5 mole) of bromobenzene,
12 g. (0.5 gram atom) of magnesium, and
500 ml. of dry ether. The dropping funnel is then replaced by an addition flask
(p. 550) which contains
38 g. (0.48 gram atom) of dry powdered black selenium (Note 5). The solution is warmed sufficiently to bring about gentle refluxing, and the
selenium is then added gradually over a period of 30 minutes at such a rate as to maintain gentle refluxing without heating. Stirring is continued for an additional 30 minutes
(Note 6).
The contents of the flask are then poured upon 600 g. of cracked ice, and, with hand stirring, 75 ml. of hydrochloric acid (sp. gr. 1.18) is added. The cold mixture is now filtered through glass wool in an ordinary funnel into a 2-l. separatory funnel. The aqueous layer is separated and extracted once with 250 ml. of ether (Note 7). The combined extract and main product are dried over 30 g. of calcium chloride, the ether is removed on a steam bath, and the residue is distilled using a 500-ml. modified Claisen flask. The selenophenol is collected at 57–59°/8 mm. or 84–86°/25 mm.; the yield is 43–54 g. (57–71%) (Note 6) and (Note 9) through (Note 14). The product should be sealed at once in a glass vial (Note 8).
2. Notes
1.
Dry
hydrogen or dry
nitrogen may be used. The gas must be oxygen-free.
Hydrogen tends to decrease the amount of oxidation to diselenide.
2.
The submitter used a simpler train consisting of two small widemouthed bottles in series closed by stoppers bearing the necessary inlet and outlet tubes constructed of 10-mm. or larger glass tubing. In each flask was a shallow layer of
50% potassium hydroxide solution; the outlet tube of the first bottle extended nearly to the surface of the solution and dipped
below the surface of the solution in the second bottle.
3.
Most selenium compounds are affected by sunlight, and many by any bright light. It is often essential to use amber glassware or to wrap the flasks in light-proof paper.
4.
Selenium compounds which contain an -SeH group are easily oxidizable in the air to diselenides. It is advantageous to replace the air by an inert gas, and to work as rapidly as possible.
5.
The
selenium is dried overnight in a
vacuum desiccator over concentrated
sulfuric acid.
6.
The higher yields of
selenophenol are favored by exclusion of air, rapid stirring, and not too rapid addition of
selenium.
7.
An alternative procedure is to extract the
selenophenol by
sodium hydroxide solution, and subsequently to acidify and extract the liberated substance. The yield of
selenophenol is not improved by employing such a procedure, but it may be of value with some compounds.
8.
The
selenophenol is water-white but rapidly turns yellow in contact with the air.
9.
The residue in the still (or alkali-insoluble material in the
ether layer if Note 6 has been employed) contains
diphenyl selenide (b.p.
167°/16 mm.) and
diphenyl diselenide (m.p.
63°). It can be separated by a combination of distillation and crystallization from
ethanol, but the amounts are small, and, unless the residues from several runs are combined, the procedure is not economical.
10.
This is a general reaction. It can be used for preparing other selenophenols whenever the desired Grignard reagent can be obtained. The submitter has made the three selenocresols,
p-bromophenylselenophenol, and
n-butylselenol by this procedure. He has also obtained thiophenols by the substitution of
sulfur for
selenium.
11.
The submitter has synthesized nine alkyl phenyl selenides in yields of 85–95% by treating
ethanol solutions of the sodium salt (the
selenophenol is dissolved in the calculated amount of
50% aqueous sodium hydroxide diluted with
ethanol) with the appropriate alkyl halide or sulfate.
12.
Many selenophenols are more advantageously prepared by hydrolysis of the aryl selenocyanate.
13.
It is well to have a
hot sulfuric-nitric acid cleaning bath in the same hood, so that apparatus need not be handled in the open laboratory. The large separatory funnel is conveniently cleaned by pouring into it
50 ml. of concentrated nitric acid. After a few minutes, the acid reacts violently with selenides remaining on the sides. The
oxides of nitrogen produced effectively clean the funnel, which can then be rinsed with water.
14.
Water-soluble selenium compounds are poured down the sink in the hood and flushed with much water.
Rubber stoppers and gloves can be freed from toxic compounds by soaking them for a few minutes in
bromine or
chlorine water and then in dilute
sodium hydroxide solution.
3. Discussion
Selenophenol has been prepared from
selenium tetrachloride and
benzene in the presence of anhydrous
aluminum chloride,
3 and by the procedure described,
4 which is a development of Taboury's.
5
This preparation is referenced from:
Appendix
Chemical Abstracts Nomenclature (Collective Index Number);
(Registry Number)
oxides of nitrogen
ethanol (64-17-5)
calcium chloride (10043-52-4)
sulfuric acid (7664-93-9)
hydrochloric acid (7647-01-0)
Benzene (71-43-2)
ether (60-29-7)
hydrogen (1333-74-0)
sodium hydroxide (1310-73-2)
magnesium (7439-95-4)
nitric acid (7697-37-2)
hydrogen cyanide (74-90-8)
bromine (7726-95-6)
nitrogen (7727-37-9)
sulfur (7704-34-9)
aluminum chloride (3495-54-3)
chlorine (7782-50-5)
potassium hydroxide (1310-58-3)
bromobenzene (108-86-1)
Phenylmagnesium bromide (100-58-3)
Diphenyl selenide (1132-39-4)
selenium
selenium tetrachloride (10026-03-6)
hydrogen selenide (7782-49-2)
Selenophenol
Benzeneselenol (645-96-5)
Diphenyl diselenide (1666-13-3)
p-bromophenylselenophenol
n-butylselenol
Copyright © 1921-, Organic Syntheses, Inc. All Rights Reserved