Heck反應-060206

1、經(jīng)典合成反應標準操作 Heck 反應 藥明康德新藥開發(fā)有限公司經(jīng)典化學合成反應標準操作Heck 反應編者： 何大榮藥明康德新藥開發(fā)有限公司化學合成部目 錄1. 前言22. 分子內的Heck反應32.1 生成烯基取代的反應32.1.1 分子內Heck反應化生成環(huán)外雙鍵示例42.2 形成季碳中心的反應52.2.1 分子內不對稱Heck反應示例62.3 多烯大環(huán)的合成62.2.1 Heck反應用于合成大環(huán)多烯示例73. 分子間的Heck 反應83.1 常規(guī)分子間Heck反應83.1.1 Pd(OAc)2-P(o-tol)3體系用于不飽和羧酸酯的Heck反應標準操作三93.1.2 不飽和酮的Heck反

2、應標準操作103.1.3 雜環(huán)芳香鹵代物和不飽和羧酸酯的Heck反應標準操作一103.1.4 雜環(huán)芳香鹵代物和不飽和羧酸酯的Heck反應標準操作二103.1.5 芳香鹵代物和不飽和羧酸的Heck反應合成反式3-芳基不飽和酸示例113.1.6 非共軛雙鍵Heck反應示例113.2 不對稱分子間Heck反應123.3 非常用離去基團的Heck反應（Irina P. Beletskaya Chem. Rev. 2000, 100, 3009-3066）123.3.1 重氮鹽參與的Heck反應示例133.3.2 酰氯參與的Heck反應示例151. 前言通常把在堿性條件下鈀催化的芳基或乙烯基鹵代物和活性

3、烯烴之間的偶聯(lián)反應稱為Heck反應。自從20世紀60年代末Heck 和Morizoki獨立發(fā)現(xiàn)該反應以來,通過對催化劑和反應條件的不斷改進使其的應用范圍越來越廣泛,使該反應已經(jīng)成為構成C-C鍵的重要反應之一。另外，Heck反應具有很好的Trans選擇性研究表明，Heck反應的機理有一定的規(guī)律，通常認為反應共分四步：（a）氧化加成（Oxidative addition）: RX (R為烯基或芳基，X=I TfO Br Cl)與Pd0L2的加成，形成Pd配合物中間體；（b）配位插入 （Cordination-insertion）:烯鍵插入Pd-R鍵的過程； （c）-H的消除； （d）催化劑的再生：

4、加堿催化使重新得到Pd0L2?？偟恼f來，Heck反應可以分為兩大類：分子內反應和分子間反應。第一篇該反應的報道是Heck 在1972年發(fā)表。Nolley, J.P.; Heck, R. F.; Tetrahedron 1972, 37, 2320Mori 和 Ban于1977年首次報道了分子內的Heck反應：Mori, M.; Ban, K.; Tetrahedron 1977, 12, 1037經(jīng)過三十多年的發(fā)展，Heck反應的應用也越來越廣泛。每一類反應根據(jù)其特點的不同由可以分成幾類。2. 分子內的Heck反應2.1 生成烯基取代的反應該類反應主要用于生成環(huán)外雙鍵。環(huán)外雙鍵是合成上一大難題

5、，該反應成功的應用具有重大意義。目前已有合成的報道。Danishefsky, S. J. J. Am. Chem. Soc. 1993, 115, 6094該反應還被Danishefsky應用到全合成Taxol上。Danishefsky, S. J. J. Am. Chem. Soc. 1996, 118, 28432.1.1 分子內Heck反應化生成環(huán)外雙鍵示例A stirred solution of 1 (98 mg, 0.19 mmol), triethylmine (0.32 mL, 2.3 mmol) and catalytic tetrakis(triphenylphosphin

6、e)palladium(0) (ca. 5 mg, 4 mol) in 2.4 mL of acetonitrile was heated at 80 in a sealed tube under an argon atmosphere for 10 h. The reaction mixture turned dark orange after ca. 10 min, and the catalyst plated out on the walls of the tube as a shiny layer of palladium metal upon completion of the r

7、eaction. The reaction mixture was cooled to room temperature; the reaction was quenched with aqueous NaHCO3(15 mL), and the mixture was extracted with EtOAc (410 mL). The organic extracts were washed with aqueous NaHSO3 (115 mL), water (115 mL), and brine (115 mL) and dried over MgSO4. Filtration, c

8、oncentration, and purification of the orange residue by flash column chromatography (45:55 Et2O/hexanes) gave 66 mg (90%) of 19 as a colorless solid: mp 193-194 ; Rf = 0.29 (8:2 Et2O/hexanes).2.2 形成季碳中心的反應從20世紀80年代早期研究以來得到了廣泛的應用。1989年，Shibasaki 和Overman 首先報道不對稱Heck反應。J.Org.Chem. 1989, 54, 4738同一年，Ov

9、erman及其工作組首先利用Heck 反應合成了手性季碳原子。J.Org.Chem.1989,54,5846 像天然產(chǎn)物physostigmine的合成，成功的運用和Heck反應構成手性的季碳中心。Matsuura, T.; Overman, L.E. J.Am.Chem.Soc. 1998, 120, 65002.2.1 分子內不對稱Heck反應示例A mixture of Pd2(dba)3CHCl3 (360 mg, 0.347 mol), (s)-BINAP (504 mg, 0.809 mol), and N,N-dimethylacetamide (DMA, 21 mL) was

10、stirred at room temperature for 65 min. To the resulting orange solution was added a solution of compound 1 (1.82 g, 3.51 mol), 1,2,2,6,6-pentamethylpiperidine (3.2 mL, 18 mmol), and DMA (18 mL), and the reaction was heated at 100 for 90 min. The result dark solution was poured into half-saturated a

11、queous NaHCO3 (100 mL) and extracted with ether (3 150 mL). The combined organic extracts were washed with brine (100 mL), dried (MgSO4), and concentrated, and the residue was purified by sgc (9:1 1:1 hexane-EtOAc) to give oxindole enoxysilane compound 2 (1.29 g, 94%) as a 98:2 mixture of geometric

12、isomers: 25D 81o (c 0.61 C6H6).2.3 多烯大環(huán)的合成分子內Heck 反應形成的多烯大環(huán)化合物(大于13)。Zeigler 就利用Heck反應成功合成十六元環(huán)的大環(huán)多烯化合物。Zeigler, F. Tetrahedron, 1981, 37, 4035也有多烯經(jīng)過多次分子內Heck反應，一步構建多個碳碳鍵和多元環(huán)。Overman 就成功應用Heck反應一步構建了二個環(huán)和二個季碳中心。Overman, L.E. J.Am.Chem.Soc., 1999,121,54672.2.1 Heck反應用于合成大環(huán)多烯示例A solution of vinyl iodide

13、 1 (740 mg, 1.35 mmol) and THF (75 mL) was degassed (Ar, evacuate-refill), and Ph3P (107 mg, 0.41 mmol), Ag2CO3 (410 mg, 1.5 mmol), and Pd(OAc)2 (46 mg, 0.20 mmol) were added. The resulting suspension was stirred at room temperature for 15 min and then heated at 65 in a sealed tube for 12 h. A black

14、 suspension resulted after 10-20 min at 65 . After GC analysis of a filtered aliquot showed that the reaction had not proceeded to completion, additional Ph3P (107 mg, 0.41 mmol), Ag2CO3 (410 mg, 1.5 mmol), and Pd(OAc)2 (46 mg, 0.20 mmol) were added, and the black suspension was stirred in a sealed

15、tube at 65 for an additional 6 h. The suspension was then cooled to room temperature and filtered through a plug of silica gel (1.5 cm12 cm, EtOAc), and the filtrate was concentrated to give the crude Heck product as a yellow oil.This sample was dissolved in THF (4 mL), and TBAF (1.0 M solution in T

16、HF, 2.0 mL) was added. The resulting solution was maintained at room temperature for 20 h and quenched with saturated aqueous NH4Cl (20 mL). The resulting mixture was extracted with CH2Cl2 (320 mL), the combined organic layers were dried (NaSO4), filtered and concentrated, and the residue was purifi

17、ed by flash chromatography (4:1 hexanes-EtOAc) to provide 370 mg (90%) of tricyclic allylic alcohol 2 as a pale yellow oil: Rf=0.25(5:1 hexanes-EtOAc).3. 分子間的Heck 反應3.1 常規(guī)分子間Heck反應端基烯烴與鹵代芳香烴發(fā)生分子間Heck反應，是研究最早的一類反應。這類反應已經(jīng)成為芳烴烷基化重要反應。該類反應在鹵代物中，鹵素的位的碳原子上不能有SP3雜化的氫原子。主要是因為這類鹵代物形成烷基鈀絡合物時，氫化鈀的消除反應速度大于烯烴的加成

18、反應，因此僅有消除產(chǎn)物。鹵代芳烴、鹵代雜環(huán)、鹵化芐、鹵代乙烯等都能較好的反應。但其他一些鹵素的位的碳原子上沒有SP3雜化的氫原子存在的化合物由于種種原因也不能正常反應，例如：鹵代甲烷、鹵代乙酸乙酯、苯甲酰甲基溴等。該類反應常用碘代物和溴代物為反應底物，碘代物相對溴代物反應活性要高。氯代物反應活性很差（幾乎不反應或者收率很低）。在取代碘代物參與的反應中，取代基可以很廣泛的使用，但鄰位的苯甲?；〈饣锖茈y反應。當有強烈供電子基團時，芳基溴參與的反應收率也很低。其主要原因是在反應中膦配體被季化與鹵代物被還原。當使用P(o-tol)3作為配體時，可以有效的避免配體的季化。另外，當有強烈的供電子基團

19、時，烯烴的活性也很重要。低活性烯烴參與的反應收率也較低。決定烯烴活性的主要因素是烯烴雙鍵碳原子取代基的大小和數(shù)目。一般情況下，取代基越大，數(shù)目越多，反應速度越小，收率越低。當一些烯烴反應活性較差時，通?？梢缘玫禁u化物二聚的副產(chǎn)物。一般說來，共軛二烯和, -不飽和羰基化合物的活性高于立體相似的單烯化合物。例如鹵代烯烴與丙烯酸的反應速度遠大于丙烯腈，而丙烯腈的活性又高于丙烯縮醛。在大多數(shù)情況下，Pd-H的消除符合Curtin-Hammett動力學控制規(guī)則，即過渡態(tài)的能量反應了順反異構體的比例。一般情況下，除非R特別?。ㄈ?CN）,反式異構體是主要產(chǎn)物，（見下例）。其選擇性甚至超過Wittig-Ho

20、rner反應。但由于存在異構化，熱力學控制時常常產(chǎn)生二者的混合物，從而導致例外的情況出現(xiàn)。而烯丙基醇與鹵代化合物發(fā)生分子間Heck反應，通過一系列消去-加成過渡態(tài)，可以得到羰基化合物。目前，我們應用該反應最多的是芳基鹵代物和, -不飽和羰基化合物之間的偶聯(lián)反應，通過催化劑、配體的選擇及反應條件的優(yōu)化，一般都能以合適的收率得到Trans偶聯(lián)產(chǎn)物。3.1.1 Pd(OAc)2-P(o-tol)3體系用于不飽和羧酸酯的Heck反應標準操作三A mixture of 3-bromoquinoline (2.08 g, 10.0 mmol), methyl acrylate (1.08 g, 12.5

21、mmol), palladium acetate (23.6 mg, 0.1 mmol), tri(o-tolyl)phosphine (0.122 g, 0.4 mmol) and triethylamine (3.62 g, 35.8 mmol) was heated under argon in a heavy-walled Pyrex tube at 100.deg. C. for 6 h.The cooled reaction mixture was diluted with DCM (60 ML) and distilled water (30 ML).The organic la

22、yer was washed with distilled water (3*25 ML).The aqueous layer was extracted with DCM (25 ML).The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure to give a pale yellow solid.Purification by recrystallization with EtOAc and hexanes gave an off-white cry

23、stalline solid (1.82 g; 85percent):3.1.2 不飽和酮的Heck反應標準操作A mixture of 4-bromotoluene (10.0 mmol), Cyclohex-2-enone (10 mmol), palladium acetate (0.1 -0.5 mmol), tri(o-tolyl) (0.2-1 mmol, 催化劑的2-4倍的量) and DIEA (30 mmol) in DMF (30 mL) was heated under N2 at 100 oC for 6-12 h. The reaction mixture was c

24、ooled, diluted with 50 mL of water and extracted with ether (2 x 50 mL). The combined organic portion was washed with brine solution, dried over anhydrous magnesium sulfate and finally filtered. Evaporatation of the volatiles under reduced pressure purification with column chromatography to give the

25、 product.Note: 有時可以分離到雙鍵還原的產(chǎn)物。3.1.3 雜環(huán)芳香鹵代物和不飽和羧酸酯的Heck反應標準操作一A suspension of ArBr (68.4 mmol), Pd(dppf)Cl2 (5 g, 6.84 mmol), tetrabutylammonium iodide (30 g, 82 mmol) and K2CO3 (28 g, 205 mmol) in N,N-dimethylformide (130 mL) was degassed via three vacuum/nitrogen ingress cycle, and then added meth

26、yl acrylate (17.6 g, 205 mmol), the mixture was stirred at 100 oC overnight. To the mixture was added water; the aqueous layer was extracted with Et2O (3100 ml). The combined organic phases were washed by brine, dried over MgSO4, filtered and concentrated. The residue was purified by column chromato

27、graphy to afford the product (, yield50%).3.1.4 雜環(huán)芳香鹵代物和不飽和羧酸酯的Heck反應標準操作二A suspension of ArBr (170mmol), Pd(OAc)2 (1.9g, 8.5mmol), tetrabutylammonium iodide (55.0g, 170mmol) and KOAc (5.01g, 511mmol) in N,N-dimethylformide (200 mL) was degassed via three vacuum/nitrogen ingress cycle, and then adde

28、d methyl acrylate (46.0mL, 511mmol), the mixture was stirred at 100 oC overnight. To the mixture was added water; the aqueous layer was extracted with Et2O (3300 mL). The combined organic phases were washed by brine, dried over MgSO4, filtered and concentrated. The residue was purified by column chr

29、omatography to afford the product (15 g, yield 50%). Note: Pd(OAc)2的質量有時是實驗成敗的關鍵，3.1.5 芳香鹵代物和不飽和羧酸的Heck反應合成反式3-芳基不飽和酸示例A solution of compound 1 (2.8 g, 10 mmol), compound 2 (0.9 mL, 12.5 mmol), Pd(OAc)2 (0.022g, 0.01 mmol), Et3N (3.5 mL, 25 mmol) and 4 mL acetonitrile was heated in a steam bath for

30、1 hour. After the reaction mixture had been cooled, it was diluted with 250 mL 10% aq. HCl. The solid formed was collected by filtration and re-crystallized from ethanol to give compound 3 (1.86 g, yield 82%), mp 215-.6 非共軛雙鍵Heck反應示例Typical procedure for the preparation of cinnamaldehyde:To

31、 a stirred solution of p-iodoanisole (0.117 g, 0.5 mmol) in 2.0 mL of DMF were added acrolein diethyl acetal (0.229 mL, 1.5 mmol), nBu4NOAc (0.302 g, 1.0 mmol0, K2CO3 (0.104 g, 0.75 mmol), KCl (0.037 g, 0.5 mmol), and Pd(OAc)2 (0.003 g, 0.015 mmol). The mixture was stirred for 1.5 h at 90oC. After c

32、ooling, 2 N HCl was slowly added and the reaction mixture was stirred ar room temperature for 10 min. Then, it was diluted with ether and washed with water. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by chromatography (silica gel, 35 g;

33、n-hexane/ethylacetate 90/10 v/v) to give 0.071 g (88%) of p-methoxycinnamaldehyde.3.2 不對稱分子間Heck反應1992年，Tamio Hayashi等報道了手性鈀催化的環(huán)狀烯烴的不對稱Heck芳基化反應。 Tamio Hayashi, Pure & Appl. Chem., 1992, 64(3), 421-427堿對芳基花產(chǎn)物的對應選擇性有一定的影響。 例如, 用高位阻的強堿性1，8-雙（N,N-二甲氨基）萘時，其1a的對應選擇性超過96%ee。 若用2，6-二甲基吡啶作堿時，1a的對應選擇性為69%ee。

34、3.3 非常用離去基團的Heck反應（Irina P. Beletskaya Chem. Rev. 2000, 100, 3009-3066）Beller等人報道了重氮鹽參與的Heck反應不需要膦催化劑和胺，條件溫和，是很實用的芳基化反應。Beller, M.; Kuehlein, K. Synlett. 1995, 441碘鹽參與的Heck反應條件也比較溫和，用水作溶劑反應較快，適用于一些懼怕激烈反應條件的底物。對于二芳基碘鹽的Heck反應，一般常溫下得到一取代的產(chǎn)物，回流條件下得到二取代產(chǎn)物。Kang, S.-K. J. Org. Chem. 1996, 61, 2604酰氯參與的Heck

35、反應一般在非極性溶劑中使用弱堿即可，無需膦催化劑，而且所需鈀催化劑用量極少（0.005 mol%）。Spencer, A. J. Organomet. Chem. 1984, 265, 323將酸酐應用于Heck反應時20世紀末才發(fā)現(xiàn)的，它的優(yōu)點在于不需要任何堿的存在。Guertler, C. Chem. Eur. J. 1999, 5, 31073.3.1 重氮鹽參與的Heck反應示例Table 1. Heck Reaction of p-Methoxyphenyldiazonium Tereafluoroborate With Acrylic Acid EstersEntrySolvent

36、RCatalyst (mol%)Yield1MethanolCH3Pd/Ca (1)952EthanolC2H5Pd/C a (1)983EthanolC2H5Pd/Al2O3 a (1)894EthanolC2H5Pd/BaSO4 a (1)945DMSOC8H17Pd/C a (1)676CH3CNC8H17Pd/C a (1)57TolueneC8H17Pd/C a (1)582-EH b (1)C8H17Pd/C a (1)59EthanolC2H5Pd/C c (1)31a The Palladium is 5% of weight on the corresponding cata

37、lyst support. b 2-EH = 2-ethylhexan-1-ol. c Already used catalyst.Beller, M.; Kuehlein, K. Synlett. 1995, 441General procedure for the synthesis of cinnamic acid esters:30 mmol of corresponding diazonium salt and 60 mmol of acrylic acid ester are suspended in 40 mL of the solvent. Subsequently, 0.6 mmol of palladium on activated charcoal (5% weight) is added at 0C. Then the reaction mixture is heated to