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Process for the preparation of donor-substituted N-formylaminoaromatics and donor-substituted formanilides

机译:供体取代的N-甲酰基氨基芳族化合物和供体取代的甲腈的制备方法

摘要

A one-step process for the preparation of donor-substituted aromatic N-formylamino compounds from donor-substituted aromatic nitro compounds and formic acid in the presence of a palladium catalyst at temperatures of approximately 0 DEG C to approximately 200 DEG C is characterised in that no further reducing agents are added. Donor-substituted aromatic N-formylamino compounds are obtained in high purity and good yield by the process according to the invention. The process makes possible a simple work-up in terms of apparatus at atmospheric pressure with simultaneous use of cost-effective materials. Using the process according to the invention, novel formanilides of the formula III are also prepared IMAGE wherein: X is NH2, NHR3, NR3R4, NHCOR3, N-morpholino, N-piperidyl, N-piperazyl, N-pyrrolidyl, N-imidazolidyl, N-pyrazolidyl and N-indolinyl, R1, R2, R3 and R4 are identical or different and are a branched or unbranched alkyl group having 1 to 12 C atoms. These compounds can be used as intermediates for the preparation of diazotype precursors.
机译:在钯催化剂的存在下,在约0℃至约200℃的温度下,由供体取代的芳族硝基化合物和甲酸制备供体取代的芳族N-甲酰氨基化合物的一步法,其特征在于:无需添加其他还原剂。通过本发明的方法以高纯度和高收率获得供体取代的芳族N-甲酰氨基化合物。该方法使得在大气压力下设备的简单后处理以及同时使用成本有效的材料成为可能。使用根据本发明的方法,还制备了式III的新的甲虫胺,其中:X是NH 2,NHR 3,NR 3 R 4,NHCOR 3,N-吗啉代,N -哌啶基,N-哌嗪基,N-吡咯烷基,N-咪唑烷基,N-吡唑基和N-吲哚基,R 1,R 2,R 3和R 4相同或不同,并且是支链的或具有1至12个碳原子的直链烷基。这些化合物可用作制备重氮型前体的中间体。

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