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Spiro phosphine-oxazoline, preparation method and application thereof

机译:螺膦-恶唑啉及其制备方法和应用

摘要

The present invention belongs to a spiro phosphine-oxazoline and preparation method and application thereof, particularly, publishes a novel spiro phosphine-oxazoline and the preparation method of its iridium complex. The substituted 7-diaryl phosphino-7′-carboxy-1,1′-Lo-dihydro-indene is used as the starting raw material to synthesize the novel spiro phosphine-oxazoline of the present invention through a two-step reaction. The novel spiro phosphine-oxazoline and the iridium precursor are complexed to become a complex, and then through ion exchange, an iridium/phosphine spiro-oxazoline complex with different anions can be obtained. The present invention overcomes the shortcomings of the existing technology. The cheap readily available amino alcohol is used as the raw material to synthesize the novel spiro phosphine-oxazoline, on the fourth position of the oxazoline ring of which there is no substitutent. The iridium complex of this novel spiro phosphine-oxazoline can catalyze the asymmetric hydrogenation of α-substituted acrylic acid, and shows very high activity and enantioselectivity, therefore has a very high research value and an industrialization prospect.
机译:本发明属于螺膦-恶唑啉及其制备方法和应用,特别是公开了新型螺膦-恶唑啉及其铱配合物的制备方法。以取代的7-二芳基膦基-7'-羧基-1,1'-Lo-二氢茚为起始原料,通过两步反应合成本发明的新型螺膦-恶唑啉。将新型螺膦-恶唑啉和铱前体复合成络合物,然后通过离子交换,可以得到具有不同阴离子的铱/膦螺-恶唑啉复合物。本发明克服了现有技术的缺点。廉价易得的氨基醇被用作合成新型螺膦-恶唑啉的原料,所述新型螺膦-恶唑啉在恶唑啉环的第四位没有取代基。该新型螺膦-恶唑啉的铱配合物可以催化α-取代丙烯酸的不对称加氢反应,并具有很高的活性和对映选择性,因此具有很高的研究价值和产业化前景。

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