36260-50-1Relevant academic research and scientific papers
Electronic effects and the stereochemistries in rearrangement-displacement reactions of triaryl(halomethyl)silanes with fluoride and with alkoxide ions
Allen, John M.,Aprahamian, Steve L.,Sans, Esther A.,Shechter, Harold
, p. 3561 - 3574 (2007/10/03)
Tetrabutylammonium fluoride (TBAF) reacts with (halomethyl)diphenyl(para-substituted-phenyl)silanes (13, X = Cl), 14 (X = Br), and 15 (X = I) in ether solvents to give fluorodiphenyl(parasubstituted-phenylmethyl)silanes (17a) and fluorophenyl(phenylmethyl)(para-substituted-phenyl)silanes (20a) by attack on silicon and migrations of the phenyl or the para-substituted-phenyl groups to C-1 with displacement of chloride ion. Sodium methoxide in dioxane effects rearrangement displacements of 14 (X = Br) to yield methoxydiphenyl(para-substituted-phenylmethyl)silanes (17b) and methoxyphenyl(phenylmethyl)(para-substituted-phenyl)silanes (20b). The migratory aptitudes of the varied phenyl groups in rearrangement-displacements of 13 with F- at 25°C are p-CF3-Ph, 2.72 > p-Cl-Ph, 1.67 > Ph, 1.00 > p-CH3-Ph, 0.91 > p-CH3O-Ph, 0.58 > p-(CH3)2N-Ph, 0.55. For reactions of 14 with sodium methoxide in dioxane, the migratory aptitudes at 23°C are p-CF3-Ph, 2.53 > p-Cl-Ph, 1.64 > Ph, 1.00 > p-CH3O-Ph, 0.84 > p-CH5-Ph, 0.79 > p-(CH3)2N-Ph, 0.68. The migratory aptitudes in the above rearrangement-displacements are increased by electron withdrawing substituents, and logarithms of the migratory aptitudes give satisfactory linear correlations with σ and/or σ-zero values of the phenyl substituents. Hammett correlations however of the migratory aptitudes from reactions of F- with 13 (X = Cl) at 0 and -20°C, 14 (X = Br) at 23, 0, and -20°C, and 15 (X = I) at 23°C are not linear. (+)-(Bromomethyl)methyl-1 naphthylphenylsilane (23, [α]D23 +8.29°, cyclohexane) reacts with CsF and with TBAF in THF to give benzylfluoromethyl-1-naphthylsilane (51, [α]D25 = 0.00°, cyclohexane) and fluoromethyl-(1 naphthylmethyl)phenylsilane (52, impure) in 10.4:1 ratio along with unchanged 23 ([α]D23 8.29°, cyclohexane). Sodium methoxide and (+)-23 in dioxane at 25°C and at 0°C yield (+)benzylmethoxymethyl-1-naphthylsilane (64) and (+)-methoxymethyl(1-naphthylmethyl)phenylsilane (65) in ～9:1 ratio. The conversions of (+)-23 to (+)-64 occur with 93% inversion about silicon. Reaction of (+)-23 with sodium methoxide at 25°C to give (+)-65 also occurs with inversion. Further, sodium ethoxide and sodium 2-propoxide react with (+)-23 at 20-25°C by rearrangement displacements on silicon with phenyl migrations to yield (+)-benzylethoxymethyl-1-naphthylsilane (69) and (+)-benzylmethyl-1-naphthyl-2-propoxysilane (70), respectively, each with 95% inversion about silicon. The mechanisms of rearrangement-displacements of 13-15 and (+)-23 by fluoride and by alkoxide ions are discussed.
USE OF SbF5 INTERCALATED IN GRAPHITE AS FLUORINATING REAGENT IN ORGANO-SILICON AND -GERMANIUM CHEMISTRY
Corriu, R.J.P.,Fernandez, J.M.,Guerin, C.
, p. 347 - 352 (2007/10/02)
The use of SbF5 intercalated in graphite as fluorinating reagent of organo-silicon and -germanium derivatives is described.While Si-O and Si-Cl bonds are readily cleaved, Si-H and Si-S bonds are only reactive in bifunctional silanes.Ge-X bonds (X=Br, Cl, OR, H) are unreactive.Allyl-silicon and allyl-germanium bonds are broken under mild conditions and in high yields, leading to the corresponding fluorosilane or fluorogermane.With bifunctional silanes, it is always possible to obtain the difluorinated derivatives.
