Functionalized cyanosilane, synthesis method and applications thereof

A technology of functional grouping and synthesis method, which is applied in the field of organic compound process application, can solve the problems of increased risk of reaction operation, low atom economy, no literature reports, etc., achieves convenient post-treatment process, wide source of raw materials, and improves synthesis efficiency Effect

Active Publication Date: 2017-02-01
EAST CHINA NORMAL UNIV
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] 2) Evans et al. used cheap HCN as a cyanide source to realize the synthesis of TMSCN in 1973. Although the yield of the reaction was high, the HCN gas greatly increased the risk of the reaction operation. The reaction process was as shown in the route in formula (II) 2 shown
[0006] 3) Sukata et al. used NaCN adsorbed by adsorption resin (XAD) in 1987 to synthesize TMSCN as a cyanogen source, and the yield was higher, but the cyanogen source NaCN used for the reaction needed to be prepared in advance, which made the operation of the reaction more cumbersome, and the reaction The atom economy of is low, and the reaction process is shown in scheme 3
[0008] Although there are so many synthetic routes to synthesize cyanosilanes, most of these methods are only used to synthesize simple cyanosilanes. For the synthesis of functionalized cyanosilanes, there is no literature report so far.

Method used

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  • Functionalized cyanosilane, synthesis method and applications thereof
  • Functionalized cyanosilane, synthesis method and applications thereof
  • Functionalized cyanosilane, synthesis method and applications thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 42

[0058] Example 42: The hydrosilylation reaction of the functionalized cyanosilane 2a synthesized in Example 4

[0059]

[0060] In a dry 25 mL Schlenk tube, add (R,R)-Salen / Al (3.0 mg, 0.005 mmol), Ph 3 PO (13.9mg, 0.05mmol), 3a (70mg, 0.5mmol) and anhydrous dichloromethane (1.0mL), the resulting mixed solution was stirred at -30°C for 0.5h, then 2a (125μL, 1.0mmol) was added, and the reaction The process was monitored by thin-layer chromatography. After the raw material 3a was consumed, 4a as shown in formula (V) could be obtained through direct column chromatography with a yield of 93%.

[0061] 2H),5.83(s,1H),2.86(s,2H),0.56(s,6H); 13 C NMR (100MHz, CDCl 3 ): δ133.9, 130.2, 128.5, 120.5, 118.4, 64.8, 37.6, -0.58;

Embodiment 43

[0062] Example 43: The hydrosilylation reaction of the functionalized cyanosilane 2a synthesized in Example 4

[0063]

[0064] In a dry 25 mL Schlenk tube, add (R,R)-Salen / Al (3.0 mg, 0.005 mmol), Ph 3 PO (41.7mg, 0.15mmol), 6a (77mg, 0.5mmol) and anhydrous dichloromethane (1.0mL), the resulting mixed solution was stirred at 25°C for 0.5h and then 2a (125μL, 1.0mmol) was added, the reaction process Monitored by thin-layer chromatography, after the raw material 6a was consumed, 7a as shown in formula (VI) could be obtained through direct column chromatography with a yield of 95%.

[0065] 2H), 2.86(s, 2H), 1.87(s, 3H), 0.59(s, 6H); 13 C NMR (100MHz, CDCl 3 ): δ134.9, 128.3, 125.5, 119.5, 118.4, 65.6, 36.7, 30.9, -0.57.

Embodiment 4

[0066] Example 44: The hydrosilylation reaction of the functionalized cyanosilane 2a synthesized in Example 4

[0067]

[0068] In a dry 25 mL Schlenk tube, add (R,R)-Salen / Al (3.0 mg, 0.005 mmol), Ph 3 PO (41.7mg, 0.15mmol), 9a (74mg, 0.5mmol) and anhydrous dichloromethane (1.0mL), the resulting mixed solution was stirred at 25°C for 0.5h and then 2a (125μL, 1.0mmol) was added, the reaction process Monitored by thin layer chromatography, after the raw material 9a was consumed, 10a as shown in formula (VII) could be obtained through direct column chromatography with a yield of 89%.

[0069] 2H),2.16(s,3H),1.78(s,3H),0.33(s,6H); 13 C NMR (100MHz, CDCl 3 ): δ142.9, 125.9, 128.5, 128.1, 120.4, 67.9, 42.5, 35.7, 27.8, 25.9, -0.57.

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Abstract

The present invention discloses a functionalized cyanosilane and a synthesis method thereof. The method comprises: adding a raw material halogenated silane and a cyanogen source MCN into an organic solvent to synthesize the functionalized cyanosilane in the absence of a catalyst or by adopting a metal salt as a catalyst. According to the present invention, the functionalized cyanosilane can participate in the reactions capable of being participated by classic TMSCN to synthesize cyanhydrin, aminoalcohol, alpha-amino cyanide compounds and other important synthesis intermediates, and can further transfer the functional group carried by the silicon protecting group into the obtained addition product in the addition reaction through the appropriate conversion so as to substantially improve the synthesis efficiency and the atomic economy of the reaction, and synthesize a variety of products impossibly synthesized by the conventional TMSCN reagents.

Description

technical field [0001] The invention belongs to the technical field of organic compound technology application, and in particular relates to functionalized cyanosilane and its synthesis method and application. Background technique [0002] Cyanosilane is an important class of cyanation reagents, which are widely used in the silicocyanation reaction of carbonyl compounds to synthesize amino alcohol compounds, and in the Strecker reaction of imine compounds to synthesize amino acid compounds. These compounds are widely found in natural compounds and drug molecules, so how to efficiently synthesize diverse cyanosilanes has been a hot topic for chemists for a long time. Taking trimethylsilyl cyanide as an example, the common synthesis methods include: [0003] 1) In 1958, Sharkey reported the use of TMSCl and AgCN to prepare TMSCN. On the one hand, the cyanide source AgCN is an expensive raw material; on the other hand, at a high temperature of 120° C. for 12 hours, only a yie...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07F7/10C07F7/18C07C49/245C07C45/51
CPCY02P20/55
Inventor 周剑曾兴平
Owner EAST CHINA NORMAL UNIV
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