Metal-catalyzed addition of phosphine and methanesulfonic acid to alkyne [9]

Full text of DOI:10.1021/ja9937728

J. Am. Chem. Soc. 2000, 122, 2387-2388
2387
Table 1. Palladium-Catalyzed Addition of PPh3 and MeSO3H to
Alkynea
Metal-Catalyzed Addition of Phosphine and
Methanesulfonic Acid to Alkyne
Mieko Arisawa and Masahiko Yamaguchi*
Department of Organic Chemistry
Graduate School of Pharmaceutical Sciences
Tohoku UniVersity, Aoba, Sendai 980-8578, Japan
ReceiVed October 21, 1999
The Wittig reaction is a powerful method of synthesizing
olefinic compounds by combining a carbonyl compound and
phosphorous ylide.1 Phosphonium salt, the precursor of the ylide,
is generally synthesized by the substitution of an organohalogen
compound with triphenylphosphine. If the salt, however, can be
prepared by the addition to an unsaturated compound, the scope
of the methodology may be considerably broadened. Unsaturated
compounds are readily available and are generally inert under
the conditions for various organic transformations in which
halogen compounds might be affected. We found an unprec-
edented addition reaction of tertiary phosphine to unactivated
alkyne catalyzed by transition metal complexes.2 The regiochem-
istry and stereochemistry can be controlled by the judicious choice
of the metal catalyst. Alkenylphosphonium salts have various
applications in synthetic chemistry,3 and several methods were
developed for their preparation: (1) stepwise dehydrogenation
of saturated phosphonium salt,4 (2) substitution of vinyl halide
or triflate with phosphine,5 and (3) electrochemical oxidation of
alkene and phosphine.6 The present method provides extremely
easy access to important organophosphorus compounds using
readily available starting materials and catalysts. It may also be
worth noting that phosphine, which is generally used as a ligand
in the transition-metal-catalyzed reaction, can form P-C bonds
with substrates.
a See the typical conditions for the reaction. b The reaction was
conducted in 50 mmol scale using 0.1 mol % of Pd(PPh3)4, and the
product was isolated as MeSO3 salt.
-
regioselectively (Markovnikov mode), and no trace of its isomer
is detected by NMR analysis of the crude product. Methane-
sulfonic acid and the palladium catalyst are essential for the
addition reaction, and no reaction occurs in their absence. With
this catalyst, the product/catalyst ratio of 500 can be attained in
a larger scale reaction (entry 2). The effect of the acid structure
is small, and benzenesulfonic acid, p-toluenesulfonic acid, p-
chlorobenzenesulfonic acid, trifluoromethanesulfonic acid, cam-
phorsulfonic acid, and even sulfuric acid can be used equally as
well. The catalytic activities of several palladium complexes are
compared: Pd(PPh3)4 (99%), Pd2(dba)3‚CHCl3 (99%), and Pd-
(OAc)2 (84%) are active, while PdCl2(PPh3)2 is inactive. This
observation may reflect the ability to form a Pd(0) complex under
the reaction conditions. While triphenylphosphine effectively
reacts with alkynes, diphenylmethylphosphine and tributylphos-
phine are inert. Various terminal alkynes react with triphenylphos-
phine to give the corresponding adducts in high yields with high
regioselectivities (entries 1-8). Hydroxy, ester, and nitrile groups
are unaffected (entries 6,7, and 8). Trimethylsilylethyne is
converted to â-trimethylsilylethenylphosphonium salt in 86% yield
(entry 9). Phosphine attacks the terminal carbon atom in this case.
When ethyne is used, 1,2-bis(triphenylphosphino)ethane is ob-
tained (entry 10), which may be formed by the conjugate addition
of phosphine to the initially generated ethenylphosphonium salt.
The internal acetylene, 4-octyne, also reacts with phosphine giving
1-Hexyne was treated with an equimolar amount of triphen-
ylphosphine and methanesulfonic acid in the presence of Pd-
(PPh3)4 (2.5 mol %) in refluxing THF for 2 h. The counteranion
was exchanged with PF6, and recrystallization gave (1-hexen-2-
yl)phosphonium salt in a quantitative yield (Table 1, entry 1).
The phosphine attacks the internal carbon atom of 1-hexyne
(1) Reviews: Maryanoff, B. E.; Reitz, A. B. Chem. ReV. 1989, 89, 863.
Kelly, S. E. Alkene Synthesis. In ComprehensiVe Organic Synthesis; Trost,
B. M., Fleming, I., Eds.; Pergamon Press: New York, 1991; Chapter 3.1,
Vol. 1, p 729.
(2) An uncatalyzed reaction of phosphine and unactivated alkyne giving
alkenylphosphine is reported: Barsegyan, S. K.; Gasparyan, G. Ts.; Ova-
kimyan, M. Zh.; Indzhikyan, M. G. J. Gen. Chem. USSR 1990, 60, 859. Metal-
catalyzed addition reaction of phosphorous compounds possessing P-H
bonds: Han, L.-B.; Hua, R.; Tanaka, M. Angew. Chem., Int. Ed. 1998, 37,
94. Addition of phosphine to activated alkynes: Nozaki, K.; Sato, N.; Ikeda,
K. Takaya, H. J. Org. Chem. 1996, 61, 4516 and references therein.
(3) For recent examples, see: Posner, G. H.; Lu, S.-B. J. Am. Chem. Soc.
1985, 107, 1424. Okada, Y.; Minami, T.; Yahiro, S.; Akinaga, K. J. Org.
Chem. 1989, 54, 974. Lee, P. H.; Kim, J. S.; Kim, Y. C.; Kim, S. Tetrahedron
Lett. 1993, 34, 7583. Byrley, I. Hewson, A. T. Tetrahedron Lett. 1994, 35,
7099. Clerici, F.; Gelmi, M. L.; Pocar, D.; Rondena, R. Tetrahedron 1995,
51, 9985. Bitterer, F.; Kucken, S.; Stelzer, O. Chem. Ber. 1995, 128, 275.
Okuma, K.; Ikari, K.; Ono, M.; Sato, Y.; Kuge, S.; Ohta, H.; Machiguchi, T.
Bull. Chem. Soc. Jpn. 1995, 68, 2313. Shen, Y.; Yao, J. J. Org. Chem. 1996,
61, 8659. Miedaner, A.; Noll, B. C.; DuBois, D. L. Organometallics 1997,
16, 5779. Hanamoto, T.; Kiguchi, Y.; Shindo, K.; Matsuoka, M.; Kondo, M.
J. Chem. Soc., Chem. Commun. 1999, 151.
(4) Schweizer, E. E.; Bach, R. D. J. Org. Chem. 1964, 29, 1746. Schweizer,
E. E.; Wehman, A. T. J. Chem. Soc. (C) 1971, 343. Saleh, G.; Minami, T.;
Ohshiro, Y.; Agawa, T. Chem. Ber. 1979, 112, 355. Okuma, K.; Ono, M.;
Ohta, H. Bull. Chem. Soc. Jpn. 1993, 66, 1308.
(5) Schweizer, E. E.; Wehman, A. T.; Nycz, D. M. J. Org. Chem. 1973,
38, 1583. Hinkle, R. J.; Stung, P. J.; Kowalski, M. H. J. Org. Chem. 1990,
55, 5033. Huang, C.-C.; Duan, J.-P.; Wu, M.-Y.; Liao, F.-L.; Wang, S.-L.;
Cheng, C.-H. Organometallics 1998, 17, 676.
(6) Ohmori, H.; Takanami, T.; Masui, M. Tetrahedron Lett. 1985, 26, 2199.
Ohmori, H.; Takanami, T.; Masui, M. Chem. Pharm. Bull. 1987, 35, 4960.
3
the (E)-adduct (entry 11), JH-P ) 23.6 Hz. The introduction of
two triphenylphosphine molecules occurs when 1,4-bis(trimeth-
ylsilyl)-1,3-butadiyne is reacted with 2.0 equiv of triphenylphos-
phine (entry 12). Here, the silyl groups are expelled during the
reaction.
When a rhodium catalyst [RhCl(cod)]2 (cod ) 1,5-cycloocta-
diene) or RhCl(PPh3)3 is used, the observed regioselectivity of
the reaction is opposite to that of the palladium-catalyzed reaction
(anti-Markovnikov mode), as shown in Table 2 (entries 1-4).
Treatment of an equimolar mixture of 4-phenyl-1-butyne, triphen-
ylphosphine, and methanesulfonic acid with [RhCl(cod)]2 (1.5
10.1021/ja9937728 CCC: $19.00 © 2000 American Chemical Society
Published on Web 02/29/2000

2388 J. Am. Chem. Soc., Vol. 122, No. 10, 2000
Communications to the Editor
Table 2. Rhodium-Catalyzed Addition of PPh3 and MeSO3H to
Alkyne
Scheme 1
Scheme 2
product was obtained in 95% yield with 78% deuteration at the
3
cis-vinyl proton of the triphenylphosphinyl group, JH-P ) 48.8
Hz (Scheme 1). H-D exchange probably takes place between
the sulfonic acid and the deuterated solvent, generating deuterated
sulfonic acid, which transferred D+ to the alkyne. Two mecha-
nisms are conceivable for the present addition reaction. One
involves the oxidative addition of the sulfonic acid to Pd(0) to
form a palladium hydride complex, which adds to the carbon-
carbon triple bonds. The reductive elimination then takes place,
resulting in the alkenylphosphonium salt.5 Alternatively, phos-
phinopalladation reaction at 1-alkyne occurs followed by pro-
todepalladation.7
Applications of the alkenylphosphonium salts in the Wittig
synthesis are shown in Scheme 2. The reaction of (3-phenyl-1-
propenyl)phosphonium salt with sodium hexamethyldisilazide
produced an ylide, and treatment with an aldehyde gave a
conjugated diene. Similarly, reaction of (1-hexen-2-yl)phospho-
nium salt yielded an unsaturated ylide via double bond migration,
which reacted with an aldehyde producing methyl-1,3-diene. An
allene was obtained from a (2-arylethenyl)phosphonium salt.
Typical procedures for the Markovnikov addition reaction are
as follows: Under an argon atmosphere, a mixture of Pd(PPh3)4
(2.5 mol %, 29 mg), triphenylphosphine (1 mmol, 262 mg),
1-hexyne (1 mmol, 0.12 mL), and methanesulfonic acid (1 mmol,
96 mg) in THF (2 mL) was heated at reflux for 2 h. Then, the
solvent was removed under reduced pressure, and the residue was
washed with ether. After the crude product was dissolved in
ethanol (2 mL), lithium hexafluorophosphate (1.5 mmol, 228 mg)
was added, and the mixture was stirred at room temperature for
1 h. The precipitated solid was collected by filtration, and the
solid was dissolved in CHCl3 followed by filtration. The solution
was concentrated, and the residue was recrystallized from CHCl3
and ether (3:1), yielding (1-hexen-2-yl)triphenylphosphonium
hexafluorophosphate (468 mg, 96%) as a colorless solid.
a Conditions A: [RhCl(cod)]2, acetone, rt, 12 h. Conditions B:
RhH(PPh3)4, acetone, refl., 12 h. b P(p-tol)3 was used. c P(p-ClC6H4)3
was used.
mol %) in acetone at room temperature for 12 h yields (E)-(4-
phenyl-1-butenyl)phosphonium salt predominantly with a small
amount of the regiosiomer in a ratio of 10:1. The isomerically
pure (E)-product is obtained by recrystallization of the PF6 salt
3
in 79% yield, JH-H ) 16.8 Hz. Under the same conditions
RhH(CO)(PPh3)3 gave only the internal adduct (37% yield). A
1:1 mixture of the regioisomers was obtained with RhH(PPh3)4
(53% yield). Use of the rhodium chloride complex appears to be
critical for the synthesis of the anti-Markovnikov product. The
reaction at room temperature is also essential to obtain the terminal
adduct predominantly, and considerable amounts of the internal
adduct are formed at higher temperatures. The regioselectivity
may be under kinetic control: An isolated terminal phosphonium
salt, (4-phenyl-1-butenyl) triphenylphosphonium salt, does not
isomerize to the internal derivative when treated with methane-
sulfonic acid in the presence of either [RhCl(cod)]2 under acetone
reflux or Pd(PPh3)4 under THF reflux. An internal phosphonium
salt, (4-phenyl-1-buten-2-yl)triphenylphosphonium salt, also does
not isomerize to the terminal compound in the presence of [RhCl-
(cod)]2 under acetone reflux.
The behavior of the conjugated alkyne slightly differs from
that of the aliphatic 1-alkyne. The addition of triphenylphosphine
to arylacetylene is effectively catalyzed by RhH(PPh3)4 (Table
2, entries 5-8), whereas Pd(PPh3)4 and [RhCl(cod)]2 are not
effective at all. The reaction is applicable to phenylacetylenes
possessing either electron-donating or electron-withdrawing groups
giving the anti-Markovnikov products. RhH(PPh3)4 catalyzes the
addition to conjugated enyne compound, yielding (1,3-alkadien-
3-yl)phosphonium salt in the Markovnikov mode (entries 9-14).
The (Z)-stereochemistry indicates the trans-addition of proton and
phosphine. Tris(p-tolyl)phosphine and tris(p-chlorophenyl)phos-
phine also yield the corresponding alkenylphosphonium salts
(entries 13 and 14).
Acknowledgment. The authors thank the Japan Society for the
Promotion of Science (RFTF 97P00302), the Ministry of Education,
Science, Sports and Culture, Japan and the Naito Science Foundation
for financial support. M.A. expresses her thanks to JSPS for a Grant-in-
Aid for Encouragement of Young Scientists (No. 11771374).
Supporting Information Available: Synthetic procedures and/or
spectral data of the products (PDF). This material is available free of
charge via the Internet at http://pubs.acs.org.
The addition of a proton and phosphine generally proceeds via
cis-addition with the exception of enynes. Accordingly, when
1-octyne was treated with methanesulfonic acid and triphen-
ylphosphine in the presence of Pd(PPh3)4 in acetone-d6, the
JA9937728
(7) Allen, A., Jr.; Lin, W. Organometallics 1999, 18, 2922.