氟化试剂:二乙胺基三氟化硫 (DAST)

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DAST二乙胺基三氟化硫,一种常用的氟化试剂。常温下是液体,在枯燥状况下室温或冰箱能临时保管,DAST在90oC会剖析,处置不妥会有爆炸的伤害。但由于操纵复杂和通用性强,DAST是利用得最普遍的氟代试剂之一。这个试剂能将羟基化合物转化为单氟代化合物,醛和酮转化为二氟代化合物[1]。

 

 

反响机理:


起首DAST会和羟基天生一其中间态,并天生一分子氟化氢。之后是氟负离子经过SN1大概SN2方法亲核打击羟基碳原子,从而天生产品[2,3]。



反响特点:

  1. 脂肪族和芬芳族的伯,仲,叔醇都能高产率的转化为响应的氟化合物。反响通常用二氯甲烷,一氟三氯甲烷等作溶剂,代替羟基通常在较高温度下反响(-78oC),代替羰基一样平常在0oC-40oC反响。

  2.  仲醇在代替的历程中会产生构型翻转,为手性分解提供了一个办法,如 (S)-2-辛醇在反响中构型完全翻转,失掉 (R)-2-氟辛烷,ee%为97.6%[4]。

 

  

文献示例:

A dry, 1-L, three-necked, round-bottomed flask is fittedwith a 500-mL dropping funnel, thermometer, a magnetic stirrer,and a reflux condenser protected from theatmosphere with a drying tube.  The apparatus is flushed with dry nitrogen, and 150 mL of dry dichloromethane and 21 mL (0.16mole) of diethylaminosulfurtrifluoride[5] are added to the flask. The contents of the flask are cooled to 10°, and a solution of 23 g (0.150 mole) of 4-nitrobenzyl alcohol in 450 mL of dichloromethane is added dropwise at a fast rate (45 minutes).  The reaction mixture is allowed to come toroom temperature and poured into a beakercontaining 300 gof ice, decomposing any unreacted diethylaminosulfurtrifluoride.  The organic layer isseparated, and the water layer is extracted twice with 45-mL portions of dichloromethane.  The organic layer andextracts are combined, washed with 150 mL of water, and dried over anhydrous magnesium sulfate. Evaporation to dryness under reduced pressure gives 20.9–22.1 g(90–95%) of crude product.  Recrystallization from 500 mL of pentane yields 15.5 g. (67%) of 4-nitrobenzyl fluoride as colorless needle-shapedcrystals, m.p. 36–37°


作者示例:

YJFX-190112-A (10.0 g, 1.0 eq.) was dissolved in CH2Cl2(100 mL), DAST (5.2 g, 1.2 eq.) was dropped slowly into the solutionunder -78 °C. The mixture was stirred for 30 min at -78 °C. The reaction waswarmmed to 30-40 °C and stirred for 1-2h.

Themixture was dropped into aq. NaHCO3 (10%, 200mL), and stirred for 20min. Extracted with CH2Cl2 (150mL*2), the organic layerwas dried with anhydrous Na2SO4 and concentrated, and the residuewas purified by column chromatography  togive product as oil (8.5 g, yield: 84%).

反响履历:

  1. 带有手性的仲醇,产生了构型翻转。

  2. 该反响滴加DAST在零下78摄氏度举行,而两头态往产品的转化却必要升温举行,因而升温时须要的(差别底物必要本人探索了)。上述反响的两头态极性和产品简直简直无差异(TLC检测无法辨别),招致最后反响做的差的缘故原由,延伸工夫后,失掉改进。

  3.  反响淬灭历程发起滴加,上述反响最开端是倒入,反响会刹时变杂,控制温度也不可,改为滴加后,失掉改进。

参考文献:

  1. Bombrun, A. et. al. J. Med. Chem. 2003, 46,4365.

  2. Rozen, S. ; Faust, Y. ; Ben-Yakov, H. Tetrahedron Lett. 1979,20, 1823.

  3. Leroy, J.; Hebert, E.; Wakselman, C. J. Org. Chem. 1979, 44,3406.

  4. Middleton, W, J. J. Org. Chem. 1975, 40, 574.

  5.  Hundlicky, M. Org. React. 1988, 34, 513.



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