Polyhalogenonitrobenzenes and derived compounds Part 5. Improved preparations of 1,2,3,4-tetrafluoro-5,6-dinitrobenzene and 3,4,5,6-tetrafluoro-1,2-phenylenediamine, and the use of the latter for the synthesis of tetrafluorobenzheterocycles
作者:Alan Heaton、Mark Hill、Frederick Drakesmith
DOI:10.1016/s0022-1139(96)03517-8
日期:1997.3
controlling the reaction by TLC monitoring and using ‘dry column’ chromatography. Compound (3) was readily converted to 1,2,3,4-tetrafluoro-5,6-dinitrobenzene (2) by peroxytrifluoroacetic acid and to 3,4,5,6-tetrafluoro-1,2-phenylenediamine (1) by SnCl2/HCl. Compound (1) was shown to be a versatile intermediate for the synthesis of tetrafluoro-benzimidazoles, -triazoles and -quinoxalines. The fungicidal
通过五氟硝基苯的胺化反应,已经加快了制备2,3,4,5-四氟-6-硝基苯胺(3)的规模,扩大了规模,并通过TLC监测和“干柱”色谱法控制了反应,提高了收率。化合物(3)易于通过过氧三氟乙酸转化为1,2,3,4-四氟-5,6-二硝基苯(2),并通过转化为3,4,5,6-四氟-1,2-苯二胺(1)。 SnCl 2 / HCl。化合物(1)被证明是用于合成四氟苯并咪唑,-三唑和-喹喔啉的通用中间体。在此报道了后者的杀真菌活性。