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1925年，A. Vilsmeier及其團(tuán)隊(duì)報(bào)道了利用POCl3和N-甲基乙酰苯胺反應(yīng)得到氯化4-氯-1,2-二甲基喹啉鹽的文章。 接著他們深入研究發(fā)現(xiàn)，N-甲基甲酰苯胺和POCl3反應(yīng)可以得到一種 氯代甲基亞胺鹽 （即是Vilsmeier試劑），此試劑可以和富電子的芳烴反應(yīng)得到苯甲醛。 利用Vilsmeier試劑在富電子芳香化合物上引入甲?；姆磻?yīng)被稱(chēng)為Vilsmeier-Haack甲?；磻?yīng)。 Vilsmeier-Haack反應(yīng)由于其條件溫和，操作簡(jiǎn)便而被廣泛用于加碳甲?；磻?yīng) 。

反應(yīng)特點(diǎn)

一、Vilsmeier試劑可以通過(guò)任何一種N,N-二取代的酰胺和酰氯(e.g., POCl3, SOCl2, 草酰氯)制得；二、最常用的Vilsmeier試劑制備方法就是利用DMF和POCl3制備得到，通常分離后使用；三、 Vilsmeier–Haack試劑是 弱親電試劑 ，對(duì)于大多數(shù)的富電子芳烴或雜環(huán)芳烴、富電子烯烴和1,3-二烯烴都可以發(fā)生此反應(yīng)；四、五元雜環(huán)芳烴的反應(yīng)活性順序：吡咯 > 呋喃 >噻吩；五、反應(yīng)溶劑通常為鹵代烴（二氯甲烷，二氯乙烷或二氯苯），DMF或POCl3和溶劑的性質(zhì)對(duì)試劑的親電性有深刻影響，因此應(yīng)慎重選擇；六、反應(yīng)溫度和反應(yīng)底物的活性有關(guān)0 °C 到80 °C不等；七、反應(yīng)的后處理前的產(chǎn)物為亞胺鹽，可以水解得到相應(yīng)的醛， H2S處理則生成硫代醛，羥胺處理則得到腈，或者還原則生成胺 ；八、反應(yīng)有區(qū)域選擇性，優(yōu)先在位阻更小的位點(diǎn)反應(yīng)（苯環(huán)對(duì)位），但是電子效應(yīng)也影響反應(yīng)位點(diǎn)的選擇；九、富電子烯烴可以發(fā)生此反應(yīng)水解后得到α,β-不飽和羰基化合物。十、-OH,-OR,-NR1R2,CH(OR)等基團(tuán)不影響反應(yīng)。

反應(yīng)機(jī)理

首先DMF和三氯氧磷反應(yīng)，生成強(qiáng)親電子的 Vilsmeier 中間體，接著芳香族化合物進(jìn)行。然后加水分解得到甲酰化產(chǎn)物。

反應(yīng)實(shí)例

【 J. Org. Chem. 1995 , 60, 2964-2965】

【 J. Org. Chem. 1997 , 62, 1083-1094】

【 Org. Lett. 2001 , 3, 2611-2613】

【 J. Org. Chem. 1992 , 57, 3636-3642】

【 Tetrahedron: Asymmetry 2000 , 11, 3375-3393】

【 J. Chem. Soc., Perkin Trans. 1， 1981 , 2662–2665】

【 Chem. Pharm. Bull. 1985 , 33, 3122–3128】

【 Eur. J. Med. Chem. 2007 , 42, 1128–1136】

In a 1L round-bottomed, three-necked flask fitted with an efficient mechanicalstirrer, a drying tube containing drierite and a 125 mL dropping funnel isplaced 288 mL (274g, 3.74moles) of freshly distilled dimethylformamide. The flask and its contents arecooled in an ice-salt bath for about 0.5 hour, and 86 mL (144g, 0.94 moles) of freshly distilledphosphorous oxychloride is subsequently added with stirring to thedimethylformamide over a period of 0.5 hour. The pinkish color of theformylation complex may be observed during this step. The 125-mL droppingfunnel is replaced with a 200 mL dropping funnel, and a solution of 100g (0.85 mole) of indole in 100 mL ofdimethylformamide is added to the yellow solution over a period of 1 hourduring which time the temperature should not rise above 10 ℃. Once the solution iswell mixed, the dropping funnel is replaced with a thermometer, and thetemperature of the viscous solution is brought to 35 ℃. The syrup is stirred efficiently atthis temperature for 1 hour, or for 15 minutes longer than is necessary for theclear yellow solution to become opaque, canary-yellow paste. At the end of thereaction period, 300 g ofcrushed ice is added to the paste with careful stirring, producing a clear,cherry-red aqueous solution.

This solution is transferred with 100 mL of water to a3-l. three-necked flask containing 200 gof crushed ice and fitted with an efficient mechanical stirrer and a separatoryfunnel containing a solution of 375 g.(9.4 mole) of sodium hydroxide in 1Lof water The aqueous base is added. The remaining two-thirds is added rapidlywith efficient stirring until about one-third of it has been added. Theremaining two thirds is added rapidly with efficient stirring, and theresulting suspension is heated rapidly to the boiling point and allowed to coolto room temperature, after which it is placed in a refrigerator overnight. Theprecipitate is collected on a filter and resuspended in 1L of water. Most of the inorganic materialdissolves, and the product is then collected on a filter, washed with three300-mL portions of water and air-dried, yielding about 120 g (97%) of indole-3-aldehyde, mp 196-197 ℃. The indole-3-aldehyderesulting from this procedure is sufficiently pure for most purposes, but itmay be recrystallized from ethanol if desired.

【 Reference: Org.Syn., Vol 4, pp 539-541. 】

Pyrophosphoryl chloride (1.889g, 7.5 mmol) was added dropwise to a stirredmixture of cold (ice bath) N,N-dimethylformamide (0.731g, 10.0 mmol) and p-dimethoxybenzene (0.691g, 5.0 mmol). The resulting syrup wasthen heated at 100 ℃for 48 hours. The cold product was basified with an aqueous solution of 2M sodium hydroxide and extracted withdichloromethane and dried (MgSO4) and concentrated. Short-path distillationgave 2,5-dimethoxybenzaldehyde (0.332g40%), mp 50-51 ℃.bp 80 ℃ at0.1 mmHg.

【 Reference: Tetrahedron ，49(19)， 4015-4034 (1993) 】

草酰氯 -DMF 體系 Vilsmeier 反應(yīng)示例

A 1-L 3-neck flask equipped with a temperaturethermocouple and an efficient overhead stirrer is charged with DMF (46.37 g, 0.63 mole) and acetonitrile (350mL). The reaction is treated dropwise with a solution of oxalyl chloride (66.12 g, 0.521 mole) in actionitrile dropwiseover 20 min so that the temperature is maintained at 20~26℃ with a water bath. Gasevolution is noted and a thick precipitate forms. The reaction is stirred atambient temperature for 1 h to insure complete conversion to the Vilsmeierreagent. The reaction is cooled in a dry-ice bath to -14?to -17?C and asolution of resorcinol (26.87 g,0.244 mole) in acetonitrile (75 mL) is added over 20 min. The Vilsmeier reagentdissolves as the reaction with resorcinol occurs, and soon afterward theprecipitation of chloride salt 4--Scheme 4 begins. The reaction is stirred at-15?C. for 35 min, then at 28~32 oC.for 2 h. The HPLC of the reaction solution shows <6% of the startingmaterial. After cooling to 3~5℃ for 2 h, the reaction is filteredand washed with cold acetonitrile (70 mL). The solid is washed with hexane(30-40 mL) and the product dried. The Vilsmeier formamidinium chloride is driedat 30~35 oC at 0.05 mmof Hg for 24 h. The recovery is 42.3 g;the yield corrected for purity is 79%; it is a single component by HPLC, mp170~173 ℃.

Hydrolysis:

To water (250 mL) stirred at 40 oC is addedthe above salt (42.3 g, 0.209mole) in three portions. The reaction is heated to 50 oC for 0.5 h,and the reaction is cooled. When the temperature had reached 35 oC,sodium thiosulfate solution (0.09M,1-2 mL) is added to discharge the resulting pink color. The reaction is cooledto 5 oC., and stirred for 2 h. The mixture is filtered, the solid iswashed with cold water, and air dried at <35 oC for 24 h giving2,4-dimethoxybenzaldehyde (24.4 g,wt/wt assay by HPLC 97%; corrected yield: 69% from resorcinol) an off-whitesolid, mp 134~136oC.

【 Reference:US5599988 】

二氯亞砜用于 Vilsmeier 反應(yīng)示例

To 108 g(0.80 mole) of N-methylformanilide cooled in an ice-water bath, 95.2 g (0.80 mole) of thionyl chloride wasadded drop by drop with stirring. After completion of the addition, the mixturewas allowed to stand at room temperature for 2 hours and then heated at 40~50 ℃ for 1 hour under areduced pressure of 60-80 mmHg. To the resulting yellow mixture, 97.6 g (0.80 mole) of1,2-methylenedioxybenzene was added and kept at 15 ℃. After completion of the addition,the reaction mixture was kept at 90 ℃ for 30 minutes, poured into icewater, and allowed to stand for 1 hour. Then, the resulting mixture wasextracted with toluene. By vacuum distillation, the toluene was removed and thedistillate at 84~85℃/30mmHg was then collected to recover unreacted 1,2-methylenedioxybenzene.Subsequently, the distillate at 131~134℃/10 mmHg was collected to obtainpiperonal. The yield (expressed in terms of mole percentage based on the amountof N-methylformanilide used) and selectivity (expressed in terms of molepercentage based on the amount of 1,2-methylenedioxybenzene having reacted) ofpiperonal were 55.6% and 95.1%, respectively.

【 Reference: US4157333 】

相關(guān)文獻(xiàn)

1. Vilsmeier, A.; Haack, A. Ber. 1927, 60, 119–122. German chemists Anton Vilsmeier and Albrecht Haack discovered this recation in 1927.

2. Reddy, M. P.; Rao, G. S. K. J. Chem. Soc., Perkin Trans. 1 1981, 2662–2665.

3. Lancelot, J.-C.; Ladureé, D.; Robba, M. Chem. Pharm. Bull. 1985, 33, 3122–3128.

4. Marson, C. M.; Giles, P. R. Synthesis Using Vilsmeier Reagents CRC Press, 1994.(Book).

5. Seybold, G. J. Prakt. Chem. 1996, 338, 392-396 (Review).

6. Jones, G.; Stanforth, S. P. Org. React. 1997, 49, 1–330. (Review).

7. Jones, G.; Stanforth, S. P. Org. React. 2000, 56, 355–659. (Review).

8. Tasneem, Synlett 2003, 138–139. (Review of the Vilsmeier–Haack reagent).

9. Nandhakumar, R.; Suresh, T.; Jude, A. L. C.; Kannan, V. R.; Mohan, P. S. Eur. J. Med. Chem. 2007, 42, 1128–1136.

10. Tang, X.-Y.; Shi, M. J. Org. Chem. 2008, 73, 8317–8320.

11. Shamsuzzaman, Hena Khanam, H.; Mashrai, A.; Siddiqui, N. Tetrahedron Lett. 2013,54, 874-877.

參考資料

一、 Strategic Applications of Named Reactions in OrganicSynthesis, László Kürti and Barbara Czakó, Vilsmeier-Haack formylation，page 688-689.

二、Name Reactions （A Collection of Detailed Reaction Mechanisms）, Jie Jack Li, Vilsmeier-Haack reaction，page 615-616.