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Hydroalumination of Alkenes and Alkynes with LiAlH<sub>4</sub> Catalyzed by [C<sub>5</sub>(CH<sub>3</sub>)<sub>5</sub>]<sub>2</sub>TiCl<sub>2</sub>
Hydroalumination of Alkenes and Alkynes with LiAlH4 Catalyzed by [C5(CH3)5]2TiCl2
Journal of the Korean Chemical Society. 2005. Jun, 49(3): 321-324
Copyright © 2005, The Korean Chemical Society
  • Received : June 14, 2004
  • Published : June 20, 2005
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형수 이
갑용 이

Abstract
Keywords
INTRODUCTION
The titanium compounds have been widely used as reagents or catalysts for organic synthesis. 1 , 2 A variety of Ti(III) and Ti(IV) compounds were reduced by various kinds of reducing agents to produce the complexes containing titanium in lower oxidation states. 3 , 4 The hydroalumination of olefins catalyzed by titanium or zirconium compounds has been developed as a convenient route to a variety of alkylaluminum compounds, however most of these reactions require long reaction time or elevated temperature. 4 , 5 In particular, TiCl 4 , ZrCl 4 , and UCl 4 are effective catalysts for the addition of lithium aluminum hydride or alane to olefinic double bonds to afford the corresponding organoaluminate or organoalane, respectively. These reactions are not only restricted to terminal olefins, but internal olefins react with LiAlH 4 . 6 It was recently reported that ZrCl 4 -catalyzed hydrostannation of alkynes with Bu 3 SnH enables to produce the trans hydrostannation product with high regio- and stereoselectivities, 7 and that the allylstannation of alkynes proceeds in the presence of catalytic amounts of ZrCl 4 or EtAlCl 3 in the trans addition manner. 8 We have directed our attention to the selective reactions of unsaturated hydrocarbons by using titanium and zirconium compounds. 9 - 11 In this paper, we describe a rapid and convenient procedure for the regioselective hydroalumination of alkenes with LiAlH 4 in the presence of [C 5 (CH 3 ) 5 ] 2 TiCl 2 , and an efficiency of the reaction was evaluated by converting the alkenes to the alkylaluminates under mild conditions. The catalytic hydroalumination of terminal alkynes to alkenes is also described together with reaction of the internal alkynes.
EXPERIMENTAL SECTION
All glassware used was predried in an oven, assembled hot and cooled with a stream of argon in glove box. All reactions were carried out under argon atmosphere. All solvents were distilled and stored over an appropriate drying agent. [C 5 (CH 3 ) 5 ] 2 TiCl 2 , and LiAlH 4 purchased from Strem Co. were used without further purification. All alkenes and alkynes were purified before use. 1 H NMR spectra were recorded in CDCl 3 on Varian Gemini-200 spectrometer with tetramethylsilane as an internal standard. Infrared spectra were measured in a KBr pellet by a Matterson Genesis II FT-IR spectrophotometer. GC analyses were carried out by a Younglin GC-600D gas chromatograph equipped with HP-5 (Hewlett Packard, 0.32 mm, 30 m) or BP-5(SGE, 0.32 mm, 60 m) capillary columns. Mass spectra were obtained by using a Shimadzu GC/MS QP-5000.
Typical procedure for hydroalumination. The mixture of [C 5 (CH 3 ) 5 ] 2 TiCl 2 (0.098 g, 0.25 mmol), LiAlH 4 (0.201 g, 5.30 mmol), and THF (15 mL) was placed in a vessel under argon. After stirring for 1 h, and allylbenzene (1.205 g, 10.2 mmol) was slowly introduced to the mixture at 0 ℃. The complete reaction was confirmed by GC, and the mixture was treated with dilute hydrochloric acid (10 mL) and extracted with n -pentane. The organic layer was dried over sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on alumina with n -pentane as an eluent, and n -pentane was removed to yield the propylbenzene (0.930 g, 76%). 1 H NMR (CDCl 3 ): δ 7.12~7.27 (m, 5H, C 6 H 5 ), 2.55 (t, 2H, CH 2 ), 1.65 (m, 2H, CH 2 ), 0.92 (t, 3H, CH 3 ). IR (cm −1 ): 3026, 2870, 1608, 1475, 1375, 753, 697.
Preparation of (2-bromoethyl)benzene. To a solution of LiAlH 4 (0.417 g, 11.0 mmol) and [C 5 (CH 3 ) 5 ] 2 -TiCl 2 (0.197 g, 0.51 mmol) in THF (20 mL) was added styrene (2.093 g, 20.1 mmol). The reaction mixture was stirred at 0 ℃ for 3 h. Bromine (7.724 g, 48.3 mmol) in diethyl ether (40 mL) was added dropwise at 0 ℃. After completion of bromine addition, the reaction mixture was allowed to remain 0.5 h at room temperature. Then the mixture was washed with 10% sodium thiosulfate solution, and saturated sodium chloride solution. The organic layer was dried over magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (n-hexane). The product was obtained (3.20 g, 86%). 1 H NMR: δ 7.17~7.31 (m, 5H C 6 H 5 ), 3.54 (t, 2H, CH 2 ), 3.14 (t, 2H, CH 2 ). IR (cm −1 ): 3062, 3028, 2964, 1602, 1453, 1262, 749, 698. Mass m/e 184 (M + ), 186 (M + +2).
Hydroalumination of diphenylethyne. The mixture of [C 5 (CH 3 ) 5 ] 2 TiCl 2 (0.104 g, 0.27 mmol), LiAlH 4 (0.201 g, 5.30 mmol), and THF (10 mL) was stirred for 1 h. Diphenylethyne (1.853 g, 10.4 mmol) in diethyl ether (10 mL) was added dropwise at 0 ℃ to the mixture, and stirred at 0 ℃ for 5 h. The reaction mixture was treated with dilute hydrochloric acid (10 mL), and extracted with n -pentane. The organic layer was dried over sodium sulfate and filtered through a short alumina column ( n -pentane) to eliminate inorganic salts. Removal of the solvents left a residue of oil and solid phase (1.80 g). GC analysis of the above residue indicated that the mixture contained cis -1,2-diphenylethene (62%), diphenylethyne (38%), and trans -1,2-diphenylethene (trace). cis -1,2-Diphenylethene (oil): 1 H NMR (CDCl 3 ): δ 7.11~7.26 (m, 10H, C 6 H 5 ), 6.59 (s, 2H, =CH-Ph). IR (cm −1 ): 3057, 1600, 1493, 1447, 992, 908.
The products are known and were characterized by comparison with authentic samples using GC and spectral data.
RESULTS AND DISCUSSION
The hydroalumination was examined with reagent systems consisting of various amounts of LiAlH 4 , 1-octene, and [C 5 (CH 3 ) 5 ] 2 TiCl 2 in THF. 11 In the same method, the reaction of 1-hexene with LiAlH 4 in the presence of catalytic amounts of [C 5 (CH 3 ) 5 ] 2 TiCl 2 in THF proceeded in a excellent yield under the reaction conditions outlined in 1 . The reactivity of Cp 2 TiCl 2 and [C 5 (CH 3 ) 5 ]TiCl 3 was compared with that of [C 5 (CH 3 ) 5 ] 2 TiCl 2 in the hydroalumination of 1-octene and styrene with LiAlH 4 , respectively. When using Cp 2 TiCl 2 and [C 5 (CH 3 ) 5 ]TiCl 3 as the catalyst, the reactions proceeded in a lower yields and a lower regioselectivity under the same conditions, and require long time (up to 24 h) or elevated temperature (65 ℃). The hydroalumination of the representative alkenes with LiAlH 4 was carried out in the presence of catalytic amounts of [C 5 (CH 3 ) 5 ] 2 TiCl 2 in THF at 0 ℃. 1 shows the results of bromination (entries 1~5) and hydrolysis (entries 6~8) of alkylhydroaluminated products of alkenes. As shown there, the reaction of terminal monosubstituted alkenes such as 1-hexene, 1-octene, styrene, and 3-phenyl-1-propene occurred at 0 ℃ in excellent yields (entries 1, 2, 5, and 7). Terminal monosubstituted alkenes have been hydroaluminated quantitatively without affecting aliphatic and aromatic functionalities. 1-Bromohexane, 1-bromooctane, and (2-bromoethyl)benzene obtained by bromination of alkylhydroaluminated products of alkenes showed a selectivity in excellent yields (entries 1, 2, and 5). The bromination results indicate that the reaction proceeds specifically to place the aluminum at the terminal carbon atom. This reagent system was also applied to the reaction of disubstituted alkenes, such as 2-octene, 2-methyl-1-propene, trans -1,2-diphenylethene, and 2-phenyl-2-propene, but reactions of these alkenes were hardly occurred at 0 ℃ even after 5 h (entries 3, 4, 6, and 8). The reaction permits the regioselective addition of LiAlH 4 to the terminal monosubstituted double bond of alkenes.
The hydroalumination of alkenesa
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a[C5(CH3)5]2TiCl2 : LiAlH4 : alkene = 1:10:20, 0 ℃. bGC yields, isolated yields in parenthesis.
The hydroalumination of alkynesa
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a[C5(CH3)5]2TiCl2 : LiAlH4 : alkyne = 1:10:20, 0 ℃. bGC yields. c,dAfter isolation, a ratio of cis/trans was determined by GC.
The hydroalumination of 1-octyne was carried out at 0 ℃, treatment of the reaction mixture with hydrochloric acid gave 1-octene (87%) and n -octane (12%). Similarly, several other alkynes were converted to the corresponding alkenes, the results are shown in 2 . The primary products of these reactions are lithium alkenylhydroaluminates which upon protonolysis afford the corresponding alkenes. In the reaction of terminal alkynes, the formation of alkanes such as ethylbenzene and n -octane was also observed, the result suggests that small amounts of dialuminates may be produced during the reaction (entries 1 and 3). 10 Moreover, in the reaction of diphenylethyne, the formation of cisdiphenylethene predominated in the initial stage, but the trans -diphenylethene was gradually increased during the reaction at 65 ℃ for 5 h ( trans/cis =18/82). The selectivity in the above hydroalumination of alkynes is higher than that in the reaction catalyzed by Cp 2 TiCl 2 . 10
In summary, the above results indicate that terminal monosubstituted alkenes can be hydroaluminated with LiAlH 4 in the presence of catalytic amounts of the [C 5 (CH 3 ) 5 ] 2 TiCl 2 under mild conditions. This reaction is rapid, and gives higher regioselectivity in excellent yields, and involves anti-Markovnikov addition. The reaction of alkynes affords preferentially monoaluminated products. In the case of internal alkynes, the formation of cis -alkenes predominates in the initial stage.
References
Wailes P. C. , Coutts R. S. P. , Weigold H. 1974 Organometallic Chemisrty of Titanium, Zirconium, and Hafnium Academic Press New York
Collman J. P. , Hegedus L. S. , Norton J. R. , Finke R. G. 1987 In Principles and Applications of Organotransition Metal Chemistry University Science Book C.A.
Eisch J. J. 1982 In Comprehensive Organometallic Chemistry; Wilkinson, G.; Stone G.; Abel, E. Ed. Vol. 1 Pergamon Press Oxford 555 - 682
Eisch J. J. 1991 In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I. Ed. Vol. 8 Pergamon Press Oxford
Sato F. , Sato S. , Sato M. 1976 J. Organometal. Chem. 122 C25 -    DOI : 10.1016/S0022-328X(00)80622-1
Sato F. , Sato S. , Kodama H. , Sato M. 1977 J. Organometal. Chem. 142 71 -    DOI : 10.1016/S0022-328X(00)91817-5
Asao N. , Liu J. , Sudoh T. , Yamamoto Y. 1995 J. Chem. Soc., Chem. Commun. 2405 -    DOI : 10.1039/c39950002405
Asao N. , Matsukawa Y. , Yamamoto Y. 1996 J. Chem. Soc., Chem. Commun. 1513 -    DOI : 10.1039/cc9960001513
Lee H. S. , Isagawa K. , Otsuji Y. 1984 Chem. Lett. 363 -    DOI : 10.1246/cl.1984.363
Lee H. S. 1987 Bull. Korean Chem. Soc. 8 484 -
Lee H. S. , Lee H. Y. 2000 Bull. Korean Chem. Soc. 21 451 -