JP2013185150A - Polystyrene supported pyridine bisoxazoline derivative-calcium catalyst - Google Patents

Abstract

PROBLEM TO BE SOLVED: To immobilize a complex to which a chiral calcium pyridine bisoxazoline derivative is coordinated.SOLUTION: As shown in chemical reaction formula (11), CaXis reacted with a pyridine bisoxazoline derivative having a polystyrene bridged structure prepared by mutually mixing at an arbitrary ratio and at random (4S,4'S,5S,5'S)-2,2' (4-vinylpyridine-2,6-diyl) bis(4,5-diphenyl-4,5-dihydroxazole), styrene and divinylbenzene (including ethyl vinyl benzene).

Description

In this invention, a pyridine bisoxazoline derivative (hereinafter referred to as Pybox) which is a neutral chiral ligand is supported on a polystyrene resin (hereinafter referred to as PS-Pybox), and a calcium salt (CaX ₂ · nH ₂ O). This complex is used for efficient asymmetric synthesis in the field of organic synthesis.

  There is an increasing demand for optically active compounds in research, development and production of functional materials such as pharmaceuticals, agricultural chemicals, and ferroelectric liquid crystals. Optical resolution methods, chiral pool methods, asymmetric synthesis methods, etc. are used as methods for obtaining the target optically active compounds. Among them, asymmetry using a complex composed of a chiral ligand and heavy metals as a catalyst is an efficient method. Examples include synthesis methods. Many successful examples of asymmetric synthesis using this chiral ligand in combination with heavy metals have been reported, and some have been put into practical use.

  On the other hand, organic synthesis reactions using Group 2 elements are well known reactions using magnesium typified by Grignard reagents, but stable metal species excluding beryllium and magnesium (Ca, Sr, Ba), Regarding so-called alkaline earth metal species, there are only a limited number of reports, and in particular, there are very few examples of enantioselective synthesis. Various chiral ligands have been studied to develop enantioselectivity.

The first successful example is an aldol reaction of an aldehyde and a ketone, catalyzed by a barium complex prepared with diisopropoxybarium Ba (O ⁱ Pr) ₂ and a chiral binaphthyl-type ligand, reported in 1998. (Non-Patent Document 1). The enantioselectivity is 50-70 ee%. Furthermore, an asymmetric aldol reaction was developed using a catalyst prepared from a chiral hydrobenzoin dialkoxide and a calcium ion as a catalyst, and the enantioselectivity was 15 to 91 ee% (Non-patent Document 2). In these reactions, an aldehyde and a ketone are directly subjected to a cross-aldol reaction, so that the product is not necessarily in a condition that the product is thermally favorably formed. In order to obtain a crossed aldol compound in a high yield, it is necessary to use a tertiary alkyl group having no active proton or an aldehyde having a bulky substituent such as a cyclohexyl group. Enantioselectivity is also good when bulky substituents are used. However, on the other hand, a problem that can be said to be a characteristic of the classic aldol reaction has been pointed out, in which the self-condensation reaction proceeds when applied to an aldehyde with little steric hindrance.

  Since 1,3-dicarbonyl compounds and iminoglycine derivatives form stable enols, many asymmetric 1,4-addition reactions of α, β-unsaturated compounds to these substrates have been reported. Chiral BINOL calcium dialkoxide is prepared by reacting chiral BINOL with potassium tert-butoxide followed by metal exchange with calcium chloride. This chiral BINOL-Ca complex catalyzes an asymmetric 1,4-addition reaction between a 1,3-dicarbonyl compound and an α, β-unsaturated ketone to give the corresponding 1,4-addition product (non- Patent Document 3). Although the reaction yield is as good as about 60 to 90%, the enantioselectivity is 0 to 88ee%, and the asymmetric induction is highly substrate-dependent, which has been pointed out as a problem.

It has been suggested that a combination of diisopropoxystrontium Sr (O ⁱ Pr) ₂ and a chiral disulfonamide ligand forms a complex in which the amide moiety is ion-bonded to strontium by alcohol exchange (Non-patent Document 4). . And strontium of this chiral complex forms a coordination bond with the carbonyl group of the 1,3-dicarbonyl compound, and activates the 1,3-dicarbonyl compound. The activated carbonyl compound rapidly undergoes an asymmetric 1,4-addition reaction with the α, β-unsaturated compound. Asymmetric induction often shows 90ee% or more, and high asymmetric induction can be led without depending on the structure of the unsaturated compound.

A chiral complex obtained by combining a chiral ligand having a bisoxazoline skeleton (hereinafter referred to as Box) and an alkaline earth metal alkoxide is an asymmetric 1,4-addition reaction between an iminoglycine derivative and an α, β-unsaturated compound. (Non-patent document 5, Patent document 1). The reaction yield is good even when any metal of Ca, Sr, and Ba is used. On the other hand, the enantioselectivity is best when Ca is used, and the selectivity decreases greatly as the Sr, Ba and atomic number increase. This is because the atomic size of Ca just fits the space of the coordination site of the Box ligand and forms a good asymmetric field, whereas in Sr and Ba, the atomic size is smaller than the coordination site. Therefore, a sufficient coordination bond distance cannot be obtained between the metal and the coordination site. For this reason, it is presumed that a sufficient asymmetric field cannot be formed, leading to a decrease in asymmetric induction (Non-patent Document 6). In the reaction between the Box ligand and Ca (O ⁱ Pr) ₂ , a Ca—N ion bond and a Ca—N coordination bond are formed between the Box ligand and the Ca metal, respectively. This suggests that Ca (O ⁱ Pr) ₂ is basic enough to draw active protons on the bridging methylene of the Box ligand.

  In the above chiral ligand-Ca complex, calcium functions as a Lewis acid. On the other hand, since the alkoxide or amide moiety of the chiral ligand functions as a Bronsted base in the catalytic reaction, it is considered that calcium cannot sufficiently exhibit the effect as a Lewis acid. In general, alkaline earth metal species have low electronegativity and their metal alkoxides are strongly basic. Furthermore, since it has many coordination sites, it is expected that higher catalytic activity can be obtained by designing neutral chiral ligands that can coordinate with these coordination sites. In order to satisfy this requirement, it is required to use a metal species having Lewis acidity that can form a sufficient coordination bond with a neutral ligand.

  From such knowledge, a catalyst system in which Pybox, which is a neutral ligand, and calcium having a large number of coordination sites are combined was examined (Non-patent Document 7, Patent Document 2). In this system, by using calcium dialkoxide, the alkoxide acts as a Bronsted base, and an asymmetric reaction field is formed when calcium is coordinated to the Pybox ligand. With this system, the addition reaction between a 1,3-dicarbonyl compound and a nitroolefin is performed with high enantioselectivity. In this catalyst system, Ca-bisallyloxide exhibits high catalytic activity. Moreover, the reaction yield is higher when the Pybox ligand is used than when it is not used. This suggests that the calcium alkoxide was more activated by the neutral ligand Pybox. In this reaction system, a Mannich reaction with an N-Boc-imine derivative (Non-patent Document 8) and an asymmetric 1,4-addition reaction using an iminoglycine derivative (Non-patent Document 9) have also been reported.

  Among alkaline earth metals, calcium is abundant in nature and has low toxicity, so it can be a very useful technique if it can be applied to organic synthesis. In particular, calcium chloride is a chemical species that is inexpensive, easily available, and very easy to handle. However, synthesis examples using calcium chloride are very limited (Non-Patent Document 10).

  Examples of organic synthesis reactions using calcium chloride include an aldol reaction between an enol silyl ether and an aldehyde (Non-Patent Document 11), and a three-component condensation reaction of an aldehyde with a primary amine and diethyl phosphite (Non-Patent Document 12). . Interestingly, in these two reactions, the chloride ion of calcium chloride serves as the Lewis base.

  As described above, the asymmetric catalytic reaction has succeeded in greatly reducing the environmental load by developing a reaction that does not use heavy metals such as alkaline earth metals. On the other hand, from the viewpoint of reducing waste, many applications have been devised for solid catalyst system by immobilizing a reaction catalyst to recover and reuse the catalyst. In the past, such techniques have been achieved by directly immobilizing metals on activated carbon or inorganic substances, but in recent years, methods using organic polymers or inorganic polymers have been widely studied.

  Silica gel and polystyrene are the most widely used immobilization carriers. Since silica gel has a large number of hydroxyl groups on its surface, a chiral solid phase carrier can be obtained by introducing a chiral ligand from these hydroxyl groups via a linker. On the other hand, in general, polystyrene is synthesized by polymerizing styrene and a styrene derivative having a coordination site site at an arbitrary ratio. In order to immobilize metals, substrates having various metal coordination sites have been introduced into polystyrene. In particular, introduction of chiral ligands can be considered for use in asymmetric synthesis, and many examples of introducing various types of chiral ligands have been reported. In particular, since the ligands of bisoxazolines represented by Pybox are planar molecules and are chemically stable, there are many examples of introducing them into polystyrene, and many solid catalyst systems have been devised. However, the metal species to be combined are heavy metals such as Yb (Non-Patent Document 13), Ru (Non-Patent Document 14-15), Cu (Non-Patent Document 16-17), Er (Non-Patent Document 18), No examples of introducing alkaline earth metals have been reported.

JP2008-253987. JP2010-207786.

Ｍ．Ａｌｅｓｓａｎｄｒｏ，Ｏ．Ｓｉｍｏｎｅｔｔａ，Ｐ．Ｄａｒｉｏ，Ｓ．Ｐｉｅｒｏ，Ｔｅｔｒａｈｅｄｒｏｎ：Ａｓｙｍｍｅｔｒｙ ２００４，１５，３２３３−３２４４． Ｗ．Ａｖｉ，Ｈ．Ｂａｒｕｃｈ，Ｐ．Ｍｏｓｈｅ，Ｊ．Ｏｒｇ．Ｃｈｅｍ．２００５，７０，４５５６−４５５９． Ｎ．Ｍａｄｈａｖａｎ，Ｗ．Ｓｏｍｍｅｒ，Ｍ．Ｗｅｃｋ，Ｊ．Ｍｏｌ．Ｃａｔａｌ．Ａ：Ｃｈｅｍ．２０１１，３３４，１−７． Yoichi M. A. Yamada, M .; Shibasaki, Tetrahedron Lett. 1998, 39, 5561-5564. T. T. et al. Suzuki, N .; Yamagiwa, Y. et al. Matsuo, S .; Sakamoto, K .; Yamaguchi, M, Shibasaki, R .; Noyori, Tetrahedron Lett. 2001, 42, 4669-4671. G. Kumaraswamy, M .; N. Sastry, N .; Jena, Tetrahedron. Lett. 2001, 42, 8515-8517. M.M. Agostinho, S .; Kobayashi, J. et al. Am. Chem. Soc. 2008, 130, 2430-2431. S. Saito, T .; Tsubogo, S .; Kobayashi, J. et al. Am. Chem. Soc. 2007, 129, 5364-5365. T. T. et al. Tsubogo, S .; Saito, K .; Seki, Y .; Yamashita, S .; Kobayashi, J. et al. Am. Chem. Soc. 2008, 130, 13321-13332. T. T. et al. Tsubogo, Y .; Yamashita, S .; Kobayashi, Angew. Chem. Int. Ed. 2009, 48, 9117-9120. T. T. et al. Poisson, T.M. Tsubogo, Y .; Yamashita, S .; Kobayashi, J. et al. Org. Chem. 2010, 75, 963-965. T. T. et al. Tsubogo, Y .; Kano, K .; Ikemoto, Y. et al. Yamashita, S .; Kobayashi, Tetrahedron: Asymmetry 2010, 21, 1221-1225. S. Harder, Chem. Rev, 3852-3876. K. Miura, T .; Nakagawa, A .; Hosomi, J. et al. Am. Chem. Soc. 2002, 124, 536-537. B. Kaboudin, H .; Zahedi, Chem. Lett. 2008, 37, 540-541. L. Stina, L .; Sergey, J .; Christina, M .; Christina, Organic Lett. 2003, 5, 3663-3665.

M.M. Alessandro, O .; Simonetta, P.A. Dario, S .; Piero, Tetrahedron: Asymmetry 2004, 15, 3233-3244. W. Avi, H .; Baruch, P.M. Moshe, J .; Org. Chem. 2005, 70, 4556-4559. N. Madhavan, W.M. Somer, M .; Weck, J .; Mol. Catal. A: Chem. 2011, 334, 1-7.

  The present inventor has so far conducted an asymmetric 1,4-addition reaction of 1,3-dicarbonyl compounds to olefins and imine derivatives having electron-withdrawing substituents using a catalyst system composed of Pybox and calcium salts. We are developing. This method is to extend the ligand to a polystyrene-supported ligand (hereinafter referred to as PS-Pybox) to form a complex bound with calcium.

（但し成分Ａ，Ｂ，Ｃ，Ｄは任意の比率であり、各成分同士の結合がランダムに混合される形態をとることで（化２）に示される部分構造を形成する。Ｒ^１、Ｒ^２はそれぞれＨまたは芳香環あるいはアルキル基であり、Ｒ^１、Ｒ^２は同一でも異なっていても良い。）

（但しｗ，ｘ，ｙ，ｚはそれぞれ独立に１以上の整数であり、任意の相手鎖と結合することでポリスチレン重合体を形成している。）The PS-Pybox ligand that is a means for solving the above problems is composed of four components represented by the following formula (1), and its partial structure is represented by the following formula (2).

(However, the components A, B, C, and D are in any ratio, and the partial structure shown in (Chemical Formula 2) is formed by taking a form in which the bonds of the components are mixed randomly. R ¹ , R ² is H, an aromatic ring or an alkyl group, and R ¹ and R ² may be the same or different.

(W, x, y, and z are each independently an integer of 1 or more, and a polystyrene polymer is formed by bonding to an arbitrary partner chain.)

Although not limited in this means, the PS-Pybox ligand is specifically formed from a component represented by the following formula (3), and the ratio is A: B: C: D = 6. : 89: 4: 1 or A: B: C: D = 13: 83: 3: 1, and it is desirable to take a form in which the bonds of the components are randomly mixed.

（但しｗ，ｘ，ｙ，ｚはそれぞれ独立に１以上の整数であり、任意の相手鎖と結合することでポリスチレン重合体を形成している。）That is, it is desirable that the partial structure of the polymer described in (0018) is represented by the following formula (4).

(W, x, y, and z are each independently an integer of 1 or more, and a polystyrene polymer is formed by bonding to an arbitrary partner chain.)

Further, calcium salts to be combined with the PS-Pybox ligand that solves the above problems are calcium salts of CaCl ₂ , CaF ₂ , CaBr ₂ , CaI ₂ , Ca (OTf) ₂ , CaCO ₃ , or water thereof. Japanese style.

Although not limited in this means, the calcium salts to be combined with the PS-Pybox ligand are specifically preferably CaCl ₂ or its dihydrate.

The complex of the present invention can be used as a catalyst in asymmetric organic synthesis. Although it is not limited, it can be used for an asymmetric 1,4-addition reaction of an olefin having an electron-withdrawing substituent and an 1,3-dicarbonyl compound represented by the following formula (5) as an example. . ≦

（但し（６）式中、Ｒ^３、Ｒ^４はそれぞれアルコキシ基、あるいはアルキル基であり、Ｒ^３、Ｒ^４は同一でも異なっていても良い。Ｒ^５はＨ、アルキル基またはハロゲン基であり、Ｒ^４とＲ^５は分子内で結合している場合も含む。）In the use example described in the above (0022), the 1,3-dicarbonyl compound that can be used is not limited, but a compound represented by the following formula (6) can be used as an example.

(In the formula (6), R ³ and R ⁴ are each an alkoxy group or an alkyl group, and R ³ and R ⁴ may be the same or different. R ⁵ is H, an alkyl group or a halogen group.) , R ⁴ and R ⁵ include the case where they are bonded within the molecule.)

（但し（７）式中、Ｒ^６はアルキル基または芳香環基または複素環基である。）In the use example described in the above (0022), the olefin having an electron-withdrawing substituent that can be used is not limited, but as an example, a compound represented by the following formula (7) can be used. .

(In the formula (7), R ⁶ represents an alkyl group, an aromatic ring group or a heterocyclic group.)

In the use examples described in the above (0022) to (0024), the reaction temperature is preferably -20 ° C. However, in the compound represented by the formula (6), when either R ³ or R ⁴ is an alkyl group, the reaction is desirably performed at −40 ° C.

  The use examples described in the above (0022) to (0024) are preferably carried out in a solvent, and although not limited, toluene can be used as a solvent. Although the reaction can be performed with hydrous toluene, it is more preferable to use anhydrous toluene or molecular sieves 4A.

In the use examples described in the above (0022) to (0024), a base is used. Although not limited, triethylamine can be used. The amount used is equimolar with the PS-Pybox ligand to be used, but in the compound represented by formula (6), when R ⁵ is a substituent other than H, triethylamine corresponding to 10 mol% is used. Is desirable.

  Hereinafter, the present invention will be clarified using examples, but the present invention is not limited to these examples.

４−ｂｒｏｍｏ−Ｎ^２，Ｎ^６−ｂｉｓ（（１Ｓ，２Ｓ）−２−ｃｈｌｏｒｏ−１，２−ｄｉｐｈｅｎｙｌｅｔｈｙｌ）ｐｙｒｉｄｉｎｅ−２，６−ｄｉｃａｒｂｏｘａｍｉｄｅ（４．００ｍｍｏｌ）と水素化ナトリウム（５５％，１２．０ｍｍｏｌ）を３０ｍＬ反応器に加え、０℃に冷却した。２１．６ｍＬのＴＨＦと２．４ｍＬのＤＭＦを加えて同じ温度を保ちながら１．５時間攪拌した。５ｍＬの飽和塩化ナトリウム水溶液をゆっくり加えて反応を停止させた後、５０ｍＬの酢酸エチルを加えて希釈した。有機層を飽和食塩水５０ｍＬで３回洗浄した後、無水硫酸ナトリウムで乾燥した。乾燥剤をろ過して濃縮して得られた残渣をショートシリカゲルカラムクロマトグラフィー（ヘキサン：酢酸エチル＝２：１）で精製することで、ピリジンビスイミダゾリン誘導体を７７％の収率で得た。
１Ｈ ＮＭＲ
（ＣＤＣｌ_３，４９５．１３ ＭＨｚ）δ：５．２６（ｄ，２Ｈ，Ｊ＝８．５Ｈｚ），５．４７（ｄ，２Ｈ，Ｊ＝８．５Ｈｚ），７．１８−７．３６（ｍ，２０Ｈ），８．５０（ｓ，２Ｈ）．
１３Ｃ ＮＭＲ
（ＣＤＣｌ_３，１５０．９２ ＭＨｚ）δ：７９．０，９０．３，１２６．２，１２６．８，１２８．０，１２８．７，１２８．９，１２９．０，１２９．７，１３５．０，１３９．４，１４０．９，１４８．０，１６２．０．Synthesis of (4S, 4'S, 5S, 5'S) -2,2 '-(4-bromopyridine-2,6-diyl) bis (4,5-diphenyl-4,5-dihydroxazole)

^{4-bromo-N 2, N} 6 -bis ((1S, 2S) -2-chloro-1,2-diphenylethyl) pyridine-2,6-dicarboxamide (4.00mmol) and sodium hydride (55%, 12. 0 mmol) was added to a 30 mL reactor and cooled to 0 ° C. 21.6 mL of THF and 2.4 mL of DMF were added and stirred for 1.5 hours while maintaining the same temperature. After slowly adding 5 mL of saturated aqueous sodium chloride solution to stop the reaction, 50 mL of ethyl acetate was added for dilution. The organic layer was washed 3 times with 50 mL of saturated brine and then dried over anhydrous sodium sulfate. The residue obtained by filtering and concentrating the desiccant was purified by short silica gel column chromatography (hexane: ethyl acetate = 2: 1) to obtain a pyridinebisimidazoline derivative in a yield of 77%.
1H NMR
(CDCl ₃ , 495.13 MHz) δ: 5.26 (d, 2H, J = 8.5 Hz), 5.47 (d, 2H, J = 8.5 Hz), 7.18-7.36 (m , 20H), 8.50 (s, 2H).
13C NMR
(CDCl ₃ , 150.92 MHz) δ: 79.0, 90.3, 126.2, 126.8, 128.0, 128.7, 128.9, 129.0, 129.7, 135.0 , 139.4, 140.9, 148.0, 162.0.

（４Ｓ，４’ Ｓ，５Ｓ，５’ Ｓ）−２，２’−（４−ｂｒｏｍｏｐｙｒｉｄｉｎｅ−２，６−ｄｉｙｌ）ｂｉｓ（４，５−ｄｉｐｈｅｎｙｌ−４，５−ｄｉｈｙｄｒｏｘａｚｏｌｅ）（３．１０ｍｍｏｌ）とＰｄ（ＰＰｈ_３）_２Ｃｌ_２（０．３１０ｍｍｏｌ）を１００ｍＬ反応器に加えた。９４ｍＬのトルエンとトリブチルビニルスズ（９．２０ｍｍｏｌ）を加え、反応液を７５℃で１時間加熱した。反応液を室温まで冷した後、反応液をセライトろ過した。ろ液をエバポレーターで濃縮することで得られる残渣に、５０ｍＬのアセトニトリルを加えて希釈した後、５０ｍＬのヘキサンを加えて分液し、さらにアセトニトリル層にヘキサン５０ｍＬを加えて分液する操作を３回繰り返す。アセトニトリル層を濃縮したものをアルミナゲルカラムクロマトグラフィー（塩基性Ａｌ_２Ｏ_３，ヘキサン：酢酸エチル＝２：１）で精製することで生成物を８０％の収率で得た。
ＩＲ （ＫＢｒ，ｃｍ^−１）
３４４２，３０６０，３０３１，２９１９，１６４２，１５９４，１４４６，１２６３，１１７７，１１０５，９６９，７５７，６９７．
１Ｈ ＮＭＲ
（ＣＤＣｌ_３，４９５．１３ ＭＨｚ）δ：５．３１（ｄ，２Ｈ，Ｊ＝８．５Ｈｚ），５．５２（ｄ，２Ｈ，Ｊ＝８．５Ｈｚ），５．６１（ｄ，１Ｈ，Ｊ＝１０．８Ｈｚ），６．１６（ｄ，１Ｈ，Ｊ＝１７．６Ｈｚ），６．７６（ｄｄ，１Ｈ，Ｊ＝１７．６，１０．８Ｈｚ），７．３０−７．３６（ｍ，２０Ｈ），８．３５（ｓ，２Ｈ）．
１３Ｃ ＮＭＲ
（ＣＤＣｌ_３，１５０．９２ ＭＨｚ）δ：７９．０，９０．１，１２０．８，１２３．６，１２６．３，１２６．９，１２７．９，１２８．６，１２８．８，１２９．０，１３３．６，１３９．７，１４１．２，１４６．６，１４７．５，１６３．１．
ＥＳＩ−ＨＲＭＳ
（ｍ／ｚ）計算値Ｃ_３７Ｈ_３０Ｎ_３Ｏ_２［Ｍ＋Ｈ］^＋：５４８．２３３３；実測値５４８．２３４３．

(4S, 4'S, 5S, 5'S) -2,2 '-(4-bromopyridine-2,6-diyl) bis (4,5-diphenyl-4,5-dihydroxazole) (3.10 mmol) and Pd (PPh ₃ ) ₂ Cl ₂ (0.310 mmol) was added to the 100 mL reactor. 94 mL of toluene and tributylvinyltin (9.20 mmol) were added and the reaction was heated at 75 ° C. for 1 hour. After cooling the reaction solution to room temperature, the reaction solution was filtered through Celite. The residue obtained by concentrating the filtrate with an evaporator was diluted by adding 50 mL of acetonitrile, followed by liquid separation by adding 50 mL of hexane, and liquid separation by adding 50 mL of hexane to the acetonitrile layer three times. repeat. The product obtained in 80% yield was obtained by purifying the concentrated acetonitrile layer by alumina gel column chromatography (basic Al ₂ O ₃ , hexane: ethyl acetate = 2: 1).
IR (KBr, cm ⁻¹ )
3442, 3060, 3031, 2919, 1642, 1594, 1446, 1263, 1177, 1105, 969, 757, 697.
1H NMR
(CDCl ₃ , 495.13 MHz) δ: 5.31 (d, 2H, J = 8.5 Hz), 5.52 (d, 2H, J = 8.5 Hz), 5.61 (d, 1H, J = 10.8 Hz), 6.16 (d, 1 H, J = 17.6 Hz), 6.76 (dd, 1 H, J = 17.6, 10.8 Hz), 7.30-7.36 (m, 20H), 8.35 (s, 2H).
13C NMR
(CDCl ₃ , 150.92 MHz) δ: 79.0, 90.1, 120.8, 123.6, 126.3, 126.9, 127.9, 128.6, 128.8, 129.0 , 133.6, 139.7, 141.2, 146.6, 147.5, 163.1.
ESI-HRMS
(M / z) Calculated value C ₃₇ H ₃₀ N ₃ O ₂ [M + H] ⁺ : 548.2333; found value 548.2343.

（４Ｓ，４’ Ｓ，５Ｓ，５’ Ｓ）−２，２’−（４−ｖｉｎｙｌｐｙｒｉｄｉｎｅ−２，６−ｄｉｙｌ）ｂｉｓ（４，５−ｄｉｐｈｅｎｙｌ−４，５−ｄｉｈｙｄｒｏｘａｚｏｌｅ）（０．１５ｍｍｏｌ）とスチレン（２．１０ｍｍｏｌ）、ジビニルベンゼン（エチルビニルベンゼンを含む）（約８４％，０．０８７ｍｍｏｌ）を０．４５ｍＬのトルエンに溶解させた。これにＡＩＢＮ（０．０１８ｍｍｏｌ）を加えた後、反応液を８０℃で２４時間加熱攪拌した。生成したポリマーをＴＨＦで洗浄し、吸引フィルターで乾燥させた。得られたポリマーを乳鉢で粉砕しＴＨＦで洗浄した後、５０℃で真空乾燥することでＰＳ−Ｐｙｂｏｘポリマーを６３％の収率で得た。Ｐｙｂｏｘの担持量は５．１ ｘ １０^−１ｍｍｏｌ／ｇ
元素分析
計算値（％）（Ｃ_９．９４Ｈ_９．５１Ｎ_０．１９Ｏ_{０．１２７}）_ｎ：Ｃ８９．３１，Ｈ７．１７，Ｎ２．００；実測値Ｃ８７．４８，Ｈ７．３１，Ｎ２．１２．

(4S, 4 ′S, 5S, 5 ′S) -2,2 ′-(4-vinylpyridine-2,6-diyl) bis (4,5-diphenyl-4,5-dihydroxylazole) (0.15 mmol) and Styrene (2.10 mmol) and divinylbenzene (including ethylvinylbenzene) (about 84%, 0.087 mmol) were dissolved in 0.45 mL of toluene. After AIBN (0.018 mmol) was added thereto, the reaction solution was heated and stirred at 80 ° C. for 24 hours. The polymer produced was washed with THF and dried with a suction filter. The obtained polymer was pulverized in a mortar and washed with THF, and then vacuum-dried at 50 ° C. to obtain a PS-Pybox polymer in a yield of 63%. The supported amount of Pybox is 5.1 × 10 ⁻¹ mmol / g.
Analysis Calculated _{(%) (C 9.94 H 9.51} N 0.19 O 0.127) n: C89.31, H7.17, N2.00; Found C87.48, H7.31, N2 12.

（４Ｓ，４’ Ｓ，５Ｓ，５’ Ｓ）−２，２’−（４−ｖｉｎｙｌｐｙｒｉｄｉｎｅ−２，６−ｄｉｙｌ）ｂｉｓ（４，５−ｄｉｐｈｅｎｙｌ−４，５−ｄｉｈｙｄｒｏｘａｚｏｌｅ）（２．４８ｍｍｏｌ）とスチレン（１６．１ｍｍｏｌ）、ジビニルベンゼン（エチルビニルベンゼンを含む）（約８４％，０．７１８ｍｍｏｌ）を３．９０ｍＬのトルエンに溶解させた。これにＡＩＢＮ（０．１５１ｍｍｏｌ）を加えた後、反応液を８０℃で２４時間加熱攪拌した。生成したポリマーをＴＨＦで洗浄し、吸引フィルターで乾燥させた。得られたポリマーを乳鉢で粉砕しＴＨＦで洗浄した後、５０℃で真空乾燥することでＰＳ−Ｐｙｂｏｘポリマーを６６％の収率で得た。Ｐｙｂｏｘの担持量は７．２ ｘ １０^−１ｍｍｏｌ／ｇである。
元素分析
計算値（％）（Ｃ_{１１．７８}Ｈ_{１０．７７}Ｎ_{０．３８４}Ｏ_{０．２５６}）_ｎ：Ｃ８７．４，Ｈ６．７１，Ｎ３．３２；実測値Ｃ８６．７，Ｈ７．０５，Ｎ３．０４．

(4S, 4 ′S, 5S, 5 ′S) -2,2 ′-(4-vinylpyridine-2,6-diyl) bis (4,5-diphenyl-4,5-dihydroxylazole) (2.48 mmol) and Styrene (16.1 mmol) and divinylbenzene (including ethylvinylbenzene) (about 84%, 0.718 mmol) were dissolved in 3.90 mL of toluene. After AIBN (0.151 mmol) was added thereto, the reaction solution was heated and stirred at 80 ° C. for 24 hours. The polymer produced was washed with THF and dried with a suction filter. The obtained polymer was pulverized in a mortar, washed with THF, and then vacuum-dried at 50 ° C. to obtain a PS-Pybox polymer in a yield of 66%. The supported amount of Pybox is 7.2 × 10 ⁻¹ mmol / g.
Elemental analysis calculated value (%) (C _11.78 H _10.77 N _0.384 O _0.256 ) _n : C87.4, H6.71, N3.32; measured values C86.7, H7.05, N3 .04.

Preparation of PS-Pybox-CaCl ₂ complex Calcium chloride (7.5 x 10 ^-3 mmol) and PS-Pybox polymer (5.2 x 10 ^-1 mmol / g, 7.5 x 10 ^-3 mmol) in a 10 mL reactor. ) Was added. 0.75 mL of toluene (undried) was added, stirred at 50 ° C. for 2 hours, and then concentrated with an evaporator. The obtained residue was vacuum-dried to obtain a calcium chloride complex of PS-Pybox polymer.

Reference example

  The usefulness of the present invention will be clarified using reference examples. Note that this is for illustrative purposes, and the utility of the present invention is not limited thereto.

Reference example 1

実施例５で得たＰＳ−Ｐｙｂｏｘポリマーの塩化カルシウム錯体にトリエチルアミン（０．０１５ｍｍｏｌ）とマロン酸メチル（０．３０ｍｍｏｌ）を加え、さらに０．７５ｍＬのトルエンを加えて−２０℃に冷却した。トランス−β−ニトロスチレン（０．３６ｍｍｏｌ）を加え、−２０℃で２４時間反応させた後、ＴＨＦで反応を希釈した。触媒をろ過した後、飽和塩化アンモニウム水溶液、１０ｍＬのジクロロメタンを加えて抽出した。水層を１５ｍＬの塩化メチレンで２回逆抽出した後、無水硫酸ナトリウムで乾燥した。乾燥剤をろ過して濃縮して得られた残渣をＰＴＬＣ（ヘキサン：酢酸エチル＝４：１）で精製することで（Ｓ）−Ｄｉｍｅｔｈｙｌ ２−（２−ｎｉｔｒｏ−１−ｐｈｅｎｙｌｅｔｈｙｌ）ｍａｌｏｎａｔｅを６９％、９３ｅｅ％で得た。
（Ｓ）−Ｄｉｍｅｔｈｙｌ ２−（２−ｎｉｔｒｏ−１−ｐｈｅｎｙｌｅｔｈｙｌ）ｍａｌｏｎａｔｅ
１Ｈ ＮＭＲ
（ＣＤＣｌ_３，５００ ＭＨｚ）δ：７．３１−７．２０（ｍ，５Ｈ），４．９２−４．８４（ｍ，２Ｈ），４．２２（ｔｄ，１Ｈ，Ｊ＝８．９，５．３Ｈｚ），３．８４（ｄ，１Ｈ，Ｊ＝８．９），３．７３（ｓ，３Ｈ），３．５３（ｓ，３Ｈ）．
１３Ｃ ＮＭＲ
（ＣＤＣｌ_３，１２４．５１ ＭＨｚ）δ：１６７．８，１６７．２，１３６．０，１２８．９，１２８．４，１２７．８，７７．３，５４．７，５２．９，５２．７，４２．９．
ＨＰＬＣ
Ｃｏｌｕｍｎ；Ｄａｉｃｅｌ Ｃｈｉｒａｌｃｅｌ ＯＤ−Ｈ， Ｓｏｌｖｅｎｔ；ｈｅｘａｎｅ／^ｉＰｒＯＨ＝７／３， ｆｌｏｗ ｒａｔｅ；０．５ｍＬ／ｍｉｎ，Ｄｅｔｅｃｔｉｏｎ；ｗａｖｅｌｅｎｇｔｈ＝２２０ｎｍ：ｔ_Ｒ＝２６．５ｍｉｎ（Ｓ），ｔ_Ｒ＝３２．３ｍｉｎ（Ｒ）．
Ｃｏｌｕｍｎ；Ｄａｉｃｅｌ Ｃｈｉｒａｌｃｅｌ ＯＤ−３， Ｓｏｌｖｅｎｔ；ｈｅｘａｎｅ／^ｉＰｒＯＨ＝７／３， ｆｌｏｗ ｒａｔｅ＝０．５ｍＬ／ｍｉｎ，Ｄｅｔｅｃｔｉｏｎ；ｗａｖｅｌｅｎｇｔｈ＝２２０ｎｍ：ｔ_Ｒ＝２２．４ｍｉｎ（Ｓ），ｔ_Ｒ＝２６．３ｍｉｎ（Ｒ）．

Triethylamine (0.015 mmol) and methyl malonate (0.30 mmol) were added to the calcium chloride complex of the PS-Pybox polymer obtained in Example 5, and further 0.75 mL of toluene was added and cooled to -20 ° C. After trans-β-nitrostyrene (0.36 mmol) was added and reacted at −20 ° C. for 24 hours, the reaction was diluted with THF. After the catalyst was filtered, a saturated aqueous ammonium chloride solution and 10 mL of dichloromethane were added for extraction. The aqueous layer was back extracted twice with 15 mL of methylene chloride and then dried over anhydrous sodium sulfate. The residue obtained by filtering the desiccant and concentrating it was purified by PTLC (hexane: ethyl acetate = 4: 1) to give (S) -dimethyl 2- (2-nitro-1-phenylethyl) malonate 69%. , 93ee%.
(S) -Dimethyl 2- (2-nitro-1-phenylethyl) malonate
1H NMR
(CDCl ₃ , 500 MHz) δ: 7.31-7.20 (m, 5H), 4.92-4.84 (m, 2H), 4.22 (td, 1H, J = 8.9, 5 .3 Hz), 3.84 (d, 1H, J = 8.9), 3.73 (s, 3H), 3.53 (s, 3H).
13C NMR
(CDCl ₃ , 124.51 MHz) δ: 167.8, 167.2, 136.0, 128.9, 128.4, 127.8, 77.3, 54.7, 52.9, 52.7 , 42.9.
HPLC
Column; Daicel Chiralcel OD-H, Solvent; hexane / ⁱ PrOH = 7/3, flow rate; 0.5 mL / min, Detection; wavelength = 220 nm: t _R = 26.5 min (S), t _R = 32.3 min (R).
Column; Daicel Chiralcel OD-3, Solvent; hexane / ⁱ PrOH = 7/3, flow rate = 0.5 mL / min, Detection; wavelength = 220 nm: t _R = 22.4 min (S), t _R = 26.3 min (R).

Claims (1)

A calcium complex having a polystyrene cross-linked structure represented by the following formula (2) in which the components A, B, C, and D represented by the following formula (1) are in an arbitrary ratio and the bonds between the components are random.

(R ¹ and R ² are each H, an aromatic ring or an alkyl group, R ¹ and R ² may be the same or different, and w, x, y and z are each independently an integer of 1 or more, (Polystyrene polymer is formed by combining with an arbitrary partner chain, and X is chloro, fluoro, bromine, iodo, trifluoromethylsulfonate, and carbonic acid.)