Generation of Silylethynolates via C-Si Bond Cleavage of Disilylketenes Induced by t-BuOK [1]

Abstract

Disilylketenes undergo selective mono-desilylation upon treatment of t-BuOK in the presence of HMPA. The resulting silylethynolates are convertible to other disilylketenes in good yields. The intermediary silylethynolate was analyzed by NMR and IR spectroscopy.

disilylketene - silylethynolate - potassium t-butoxide - carbon-silicon bond cleavage - HMPA

References

<A NAME="RU00702ST-1">1</A>

Presented in part at the 70th Annual Meeting of the Chemical Society of Japan, Tokyo, March 1996, Abstr. 2J392.

<A NAME="RU00702ST-2">2</A>

Deceased Oct. 4, 1995. Address all correspondence to Dr. Masato Ito, Department of Applied Chemistry, Graduate School of Science and Engineering, Tokyo Institute of Technology, 2-12-1 O-okayama, Meguro-ku, Tokyo 152-8552, Japan; E-mail: [e-mail].

<A NAME="RU00702ST-3">3</A> Ito M. Shirakawa E. Takaya H. Synlett  1996,  635 

For reviews on the chemistry of ynolates, see:

<A NAME="RU00702ST-4A">4a</A> Stang PJ. Zhdankin VV. In The Chemistry of Triple-bonded Functional Groups   Patai S. John Wiley & Sons; Chichester: 1994.  p.1136-1145  

<A NAME="RU00702ST-4B">4b</A> Shindo M. Chem. Soc. Rev.  1998,  27:  367 

<A NAME="RU00702ST-5A">5a</A> Kai H. Iwamoto K. Chatani N. Murai S. J. Am. Chem. Soc.  1996,  118:  7634 

<A NAME="RU00702ST-5B">5b</A> Akai S. Kitagaki S. Naka T. Yamamoto K. Tsuzuki Y. Matsumoto K. Kita Y. J. Chem. Soc., Perkin Trans. 1  1996,  1705 

<A NAME="RU00702ST-5C">5c</A> Iwamoto K. Kojima M. Chatani N. Murai S. J. Org. Chem.  2001,  66:  169 

<A NAME="RU00702ST-6A">6a</A> Sakurai H. Shirahata A. Sasaki K. Hosomi A. Synthesis  1979,  740 

<A NAME="RU00702ST-6B">6b</A> Efimova IV. Kazankova MA. Lutsenko IF. Zh. Obshch. Khim.  1985,  55:  1647 

<A NAME="RU00702ST-7">7</A> Recently, Ishikawa and co-workers reported (Me₃Si)₃SiLi undergoes nucleophilic attack onto the silicon center of 1a in THF, but their attempts to trap the resulting silylethynolate were unsuccesful: Naka A. Ohshita J. Kunai A. Lee ME. Ishikawa M. J. Organomet. Chem.  1999,  574:  50 

<A NAME="RU00702ST-8A">8a</A> n-BuLi is known to react with 1a at the ketene sp-carbon in the absence of HMPA: Ponomarev SV. rman MB. Lebedev SA. Pechurina SY. Lutsenko IF. Zh. Obsh. Khim.  1971,  41:  127 

<A NAME="RU00702ST-8B">8b</A> Also see: Woodbury RP. Long NR. Rathke MW. J. Org. Chem.  1978,  43:  376 

<A NAME="RU00702ST-8C">8c</A> For the reaction of phosphorous ylides with 1a or 1b leading to mono-silylated allenes, see: Kita Y. Tsuzuki Y. Kitagaki S. Akai S. Chem. Pharm. Bull.  1994,  42:  233 

Analytical data for 2:

<A NAME="RU00702ST-9A">9a</A>

1,1-Bis(trimethylsilyl)-2-[(1,1-dimethylethyl)dimethylsilyl]oxy-2-phenylethene (2, R = Ph). ¹H NMR (CDCl₃) δ: -0.31 (s, 9 H), -0.29 (s, 6 H), 0.25 (s, 9 H), 0.86 (s, 9 H), 7.18-7.29 (m, 5 H); ¹³C NMR (CDCl₃) δ: -3.1, 2.1, 2.4, 18.6, 26.3, 109.9, 127.8, 128.0, 129.6, 142.0, 165.9. Anal. Calcd for C₂₀H₃₈OSi₃: C, 63.42; H, 10.11. Found: C, 63.31; H, 10.35.

<A NAME="RU00702ST-9B">9b</A>

1,1-Bis(trimethyl-silyl)-2-[(1,1-dimethylethyl)dimethylsilyl] oxy-1-propene (2, R = Me). This compound was not obtained in pure form and thus only ¹H and ¹³C NMR spectral data were shown.
¹H NMR (CDCl₃) δ: 0.12 (s, 9 H), 0.14 (s, 9 H), 0.20 (s, 6 H), 0.95 (s, 9 H), 2.03 (s, 3 H); ¹³C NMR (CDCl₃) δ: -2.3, 0.1, 2.7, 2.9, 19.1, 26.5, 107.1, 164.5.

<A NAME="RU00702ST-10">10</A> Rathke’s report on the isolation of 1a by warming a THF solution of lithio t-butyl bis(trimethylsilyl)acetate to 25 °C may indicate that the eliminated t-BuOLi does not undergo C-Si bond cleavage of 1a under their condition: Sullivan DF. Woodbury RP. Rathke MW. J. Org. Chem.  1977,  42:  2038 

<A NAME="RU00702ST-11A">11a</A>

General Procedure for the Preparation of Disilylketenes using t -BuOK: Preparation of [(1,1-dimethylethyl)dimethylsilyl](trimethylsilyl)ketene(1b) from 1a is representative. Disilyllketene 1a (296.5 mg, 1.59 mmol) was dissolved in THF (1.6 mL) and HMPA (0.28 mL, 1.61 mmol). To the resulting yellow solution was added a solution of t-BuOK (180.0 mg, 1.60 mmol) in THF (3.2 mL) at 0 °C. The mixture was stirred for 1 h at the same temperature and quenched by t-BuMeSiOTf (0.37 mL, 1.61 mmol). After stirring the resulting solution for 2 h at room temperature, the reaction mixture was diluted with pentane and washed with water. Then the organic layer was dried by Na₂SO₄ and filtered through Florisil. Evaporation of the solvent followed by silica-gel chromatography (Wakogel C-200) afforded 1b as a colorless oil (305.4 mg, 84% yield).

<A NAME="RU00702ST-11B">11b</A>

We were unable to detect the formation of any
O-silylated product (silyl silylethynyl ether) under these conditions. See ref. [13c] .

<A NAME="RU00702ST-11C">11c</A>

The use of carbon electrophiles (MeI, Me₂SO₄, Me₃OBF₄, or PhCHO) instead of R₃SiX resulted in the formation of intractable mixtures under similar conditions.

Analytical data for new disilylketenes (silicon-attached quarternary carbon was not observed in ¹³C NMR spectra):

<A NAME="RU00702ST-12A">12a</A>

(Dimethylphenylsilyl)(trimethylsilyl)ketene(1d). ¹H NMR (CDCl₃) δ: 0.14 (s, 9 H), 0.52 (s, 6 H), 7.40-7.43 (m, 3 H), 7.59-7.63 (m, 2 H); ¹³C NMR (CDCl₃) δ: -0.2, 1.2, 127.8, 129.4, 133.6, 138.3, 166.9; IR(neat) 2084 cm^-1 (CCO); MS (70 eV) m/z 248 (M⁺); bp 62-70 °C (0.05 mmHg). Anal. Calcd for C₁₃H₂₀OSi₂: C, 62.84; H, 8.11. Found: C, 63.10; H, 8.28.

<A NAME="RU00702ST-12B">12b</A>

Bis(triphenylsilyl)ketene(1k). ¹H NMR (CDCl₃) δ: 7.21-7.49 (m, 30 H); ¹³C NMR (CDCl₃) δ: 127.7, 127.8, 129.7, 129.8, 133.7, 135.2, 135.4, 135.9, 166.2; IR(nujol) 2080 cm^-1 (CCO); MS (70 eV) m/z 558 (M⁺); mp 165-166 °C. Anal. Calcd for C₃₈H₃₀OSi₂: C, 81.67; H, 5.41. Found: C, 81.40; H, 5.32.

<A NAME="RU00702ST-13A">13a</A> Ponomarev SV. Zolotareva AS. Ezhov RN. Kuznetsov YV. Petrosyan VS. Russ. Chem. Bull.  2001,  50:  1093 

<A NAME="RU00702ST-13B">13b</A> Ponomarev SV. Zolotareva AS. Leont’ev AS. Kuznetsov YV. Petrosyan VS. Russ. Chem. Bull.  2001,  50:  1088 

<A NAME="RU00702ST-13C">13c</A> Groh BL. Magrum GR. Barton TJ. J. Am. Chem. Soc.  1987,  109:  7568 

<A NAME="RU00702ST-13D">13d</A> Buncel E. Edlund TKVU. J. Organomet. Chem.  1992,  437:  85 

<A NAME="RU00702ST-13E">13e</A> Pons J.-M. Kocienski P. Tetrahedron Lett.  1989,  30:  1833 

<A NAME="RU00702ST-13F">13f</A> Grishin YK. Ponomarev SV. Lebedev SA. Zh. Org. Khim.  1974,  10:  404 

<A NAME="RU00702ST-13G">13g</A> Valent’ E. Perics MA. Serratosa F. J. Org. Chem.  1990,  55:  395 

<A NAME="RU00702ST-13H">13h</A> Stang PJ. Roberts KA. J. Am. Chem. Soc.  1986,  108:  7125 

<A NAME="RU00702ST-13I">13i</A> Pericàs MA. Serratosa F. Valent’ E. Tetrahedron  1987,  43:  2311 

<A NAME="RU00702ST-14">14</A> Bassindale AR. Glynn SJ. Taylor PG. In The Chemistry of Organic Silicon Compounds   Part 1, Vol. 2:  Rappoport Z. Apeloig Y. John Wiley & Sons; Chichester: 1998.  Chap. 7.

<A NAME="RU00702ST-15A">15a</A> Examples for a related alkali metal alkoxide-induced C-Si bond cleavage reaction: Sakurai H. Nishiwaki K. Kira M. Tetrahedron Lett.  1973,  42:  4193 ; see also ref. 13d

<A NAME="RU00702ST-15B">15b</A>

We suppose that HMPA may coordinate onto the smaller silicon center of the disilylketene to form a penta-coordinate silicate, and facilitate the alkoxide-induced Si-C bond cleavage.