Organic Syntheses, Coll. Vol. 6, p.722 (1988); Vol. 52, p.115 (1972).
Caution! Nickel carbonyl
is a flammable, volatile (b.p. 43°
), highly toxic reagent. Safety glasses, gloves, and an apron should be worn when handling this reagent and the first step of this preparation should be conducted in an efficient hood (Note 1)
has been identified as a carcinogen; OSHA has issued emergency standards on its use. All procedures involving benzene
should be carried out in a well-ventilated hood
, and glove protection is required.
A 1-l., three-necked flask is equipped with a reflux condenser, a pressure-equalizing dropping funnel, a three-way stopcock, and a large magnetic stirring bar
. The system is flushed with argon (Note 2)
, and 380 ml. of benzene (Note 3)
is placed in the flask. From an inverted lecture cylinder 50.8 g. (38.5 ml., 0.298 mole) of nickel carbonyl (Note 4)
is introduced into the addition funnel. The nickel carbonyl
is added to the benzene
while an atmosphere of argon
is maintained, and the flask is immersed in an oil bath
at 50°. With a syringe, 10.04 g. (0.07437 mole) of methallyl bromide (Note 5)
is added over 10 minutes. After a short induction period, evolution of carbon monoxide
becomes rapid and a deep red color appears. The exit gas is led from the top of the condenser through a gas bubbler tube
to monitor the rate of gas evolution. As the gas evolution becomes vigorous, the bath temperature is raised to 70° and maintained at this temperature for 30 minutes after gas evolution ceases (the total time after addition of methallyl bromide
is 1.5 hours). The resulting solution is allowed to cool to 25°, and the benzene
and excess nickel carbonyl
are removed under reduced pressure (water aspirator
), applying an oil bath at 30° as needed to maintain a rapid rate of evaporation (Note 6)
. The residual, red, solid π-methallylnickel bromide
(>85%) is used directly in the next step (Note 7)
A solution of 9.95 g. (0.0634 mole) of bromobenzene (Note 8)
in 100 ml. of oxygen-free N,N-dimethylformamide
is added, under an argon
atmosphere at 25°, to a solution of the crude nickel complex (an 85%
yield is assumed) in 65 ml. of oxygen-free N,N-dimethylformamide
, over a 15-minute period. After the addition is complete, the reaction mixture is stirred at 25° for 12 hours, then warmed to 60° for one hour. Complete reaction of the nickel complex is indicated by a red to emerald green color change, characteristic of a solution of nickel dibromide
. After being cooled to 25°, the solution is poured into a mixture of 250 ml. of water and 250 ml. of petroleum ether
); 2 ml. of 12 M hydrochloric acid
is added (Note 10)
, and the mixture is filtered through Celite filter aid, facilitating separation of the layers. The organic layer is separated, washed with two 100-ml. portions of water, dried over anhydrous magnesium sulfate
, and concentrated with a rotary evaporator
at water aspirator pressure, affording 8.0–9.6 g.
of a clear, colorless liquid. Distillation through a short Vigreux column
gives 5.58–6.02 g.
yield based on bromobenzene
) of methallylbenzene
as a colorless liquid, b.p. 67–68° (19 mm.)
1.5064 (Note 11)
is preferred by the submitters for its high density which allows opening of the reaction vessel without significant displacement of the inert atmosphere by air. A nitrogen
atmosphere was used by the checkers and was equally effective in preventing oxidation of the π-allylnickel complex.
Anhydrous, air-free benzene
was prepared by distillation under argon
, discarding a 20% forerun. The checkers used benzene from a freshly opened bottle (Fisher Scientific Company)
Nickel carbonyl, available from Matheson Gas Products
, was used by the checkers.
is prepared from methallyl chloride (Eastman Organic Chemicals)
with a halide exchange reaction. A solution of 148.3 g. (1.639 moles) of methallyl chloride
and 213.8 g. (2.460 moles) of lithium bromide
in 1 l. of dry acetone
is refluxed for 5 hours. The mixture is filtered, and the filtrate is distilled through a 30-cm. Vigreux column
, affording 69.2 g.
) of methallyl bromide
, b.p. 88–93°
1.4672. The purity was 98 ± 2% by GC analysis on a 20% Carbowax column
is drawn into the aspirator flow during this operation. In many laboratories the hood
plumbing is connected with the general plumbing line, and vapors of highly toxic nickel carbonyl
may diffuse back to sinks at the laboratory bench. If such an arrangement is suspected, the solvent and excess nickel carbonyl
can be collected by employing a cold trap
(−78° or −196°) between the reaction mixture and the aspirator. Care should be used in the disposal of this mixture.
Pure π-methallylnickel bromide
can be obtained by dissolving the residue in 150 ml. of oxygen-free anhydrous diethyl ether
, filtering under argon
, concentrating the filtrate until crystals begin to form, and cooling at −78° for 12 hours. The crystals are isolated by removing the liquid via
suction through a syringe needle
under a positive pressure of argon
, yielding 12.1 g.
) of dark-red crystals. The 1
H NMR spectrum can be obtained only by rigorous exclusion of oxygen
from the sample and filtration of the sample as the last stage of sample preparation. The 1
H NMR spectrum (C6
) shows three singlets at δ 2.07 (3H), 2.82 (2H), and 2.83 (2H).
Bromobenzene was used as supplied by Aldrich Chemical Company, Inc.
Purification by distillation under argon
did not change the yield of methallylbenzene
. The checkers used the product available from Eastman Organic Chemicals (white label).
was distilled from calcium hydride
at 71° (32 mm.) and stored under argon
. The checkers used a freshly opened bottle of the product (white label grade) available from Eastman Organic Chemicals.
The hydrochloric acid
solution is added to speed solution of the nickel salts, which would otherwise lead to emulsions during separation. If no emulsion is encountered after mixing the petroleum ether and water solutions, no hydrochloric acid
need be added. Similarly, the filtration through Celite filter aid
is intended to remove finely divided nickel
metal and other insoluble particles which complicate the washing procedure. If no particles are present, the filtration step should be omitted.
The product consists of 99% methallylbenzene
and 1% 2,5-dimethyl-1,5-hexadiene
, by 1
H NMR analysis. The 1
H NMR spectrum of methallylbenzene
) shows peaks at δ 1.63 (broad s, 3H, allylic CH3
), 3.25 (broad s, 2H, allylic CH2
), 4.75 (m, 2H, C=CH2
), and 7.15 (s, 5H, C6H5
). The 1
H NMR spectrum of 2,5-dimethyl-1,5-hexadiene
) shows peaks at δ 1.70 (broad s, 6H, 2CH3
), 2.12 (broad s, 4H, 2 allylic CH2
), and 4.75 (m, 4H, 2CH2
=C). A small forerun contained 0.30 g.
yield) of methallylbenzene
and a larger quantity of 2,5-dimethyl-1,5-hexadiene
. The distillation residue is composed of 0.24–0.34 g.
yield) of methallylbenzene
and 0.38–0.52 g.
yield) of biphenyl
. The distillation fractions may be analyzed by GC with a 180 cm. by 6.4 mm. column packed with 10% SE-30 on Chromosorb G
. The retention times for methallylbenzene
are 4.0 minutes and 2.0 minutes, respectively, at 125°.
The preparation illustrates the procedure for formation of π-allylnickel halides and their reaction with aryl halides.9
The complexes can be obtained from allylic chlorides, bromides, and iodides10,11,12
even when the allylic halides bear alkyl, carboalkoxyl, or alkenyl side chains.11
The coupling step is generally applicable to aryl, alkyl, and vinyl bromides or iodides;9
organic chlorides are usually unreactive with π-allylnickel halides. Other polar aprotic solvents (hexamethylphosphoric triamide, dimethyl sulfoxide, N-methylpyrrolidone
) have been used.13
Protic solvents lead to the destruction of the π-allylnickel complex by slow protonation of the allyl ligand.13
No reaction occurs between aryl, alkyl, or vinyl halides and π-allylnickel bromide in less polar solvents such as tetrahydrofuran
, or hydrocarbons. The π-allylnickel bromide complexes are very reactive with allyl halides, but halogen–metal exchange precedes coupling and a mixture of products is obtained as illustrated in the following example.14
The π-allylnickel complex from trans-geranyl bromide
reacts with alkyl halides, giving a mixture of cis
the double bond that participates in the π-allyl group is isomerized during the sequence of reactions:
reacts with π-methallylnickel bromide
, producing a mixture of epimeric 4-methallylcyclohexanols.9
Note that the hydroxyl group has no significant effect on this reaction.
The advantages of π-allylnickel halides reside in their nonnucleophilic and nonbasic character which allow especially selective reactions with organic halides in the presence of a large number of other functional groups. Carbonyl and hydroxyl groups react much more slowly than organic halides (especially iodides) with π-allylnickel halides, while olefins, nitriles, alkyl chlorides, and aromatic hydrocarbons are inert to these reagents.9,13
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