Recommanded Product: N-tert-ButoxycarbonylhydroxylamineIn 2022 ,《Metal-Free Direct Transformation of Aryl Boronic Acid to Primary Amines》 appeared in European Journal of Organic Chemistry. The author of the article were Kumar, Puneet; Verma, Saumya; Rathi, Komal; Chandra, Dinesh; Prakash Verma, Ved; Jat, Jawahar L.. The article conveys some information:
In this work, a transition-metal free approach for the construction of primary aromatic amines R/R1NH2 (R = 4-chlorophenyl, 2H-1,3-benzodioxol-5-yl, naphthalen-2-yl, etc.)/(R1 = Ph, 4-methylphenyl, 4-hydroxyphenyl, 4-chlorophenyl, 2-cyanophenyl) from aryl boronic acids RB(OH)2 and esters R1Bpin with N-Boc-O-tosylhydroxylamine as an amine surrogate was reported. Bench stable TsONHBoc is easy to use and it produces a non-interfering water-soluble byproduct. The protocol is operative for both electron-rich and electron-deficient aryl boronic acids under acidic conditions, wherein, the former arenes affords a better yield of the desired product. Even, sterically hindered and halogenated substrates are easily amenable under this reaction condition. The current protocol can be scaled up to produce gram-scale primary aromatic amines. In the part of experimental materials, we found many familiar compounds, such as N-tert-Butoxycarbonylhydroxylamine(cas: 36016-38-3Recommanded Product: N-tert-Butoxycarbonylhydroxylamine)
N-tert-Butoxycarbonylhydroxylamine(cas: 36016-38-3) belongs to anime. Hydrogen peroxide (H2O2) and peroxy acids generally add an oxygen atom to the nitrogen of amines. With primary amines, this step is normally followed by further oxidation, leading to nitroso compounds, RNO, or nitro compounds, RNO2. Secondary amines are converted to hydroxylamines, R2NOH, and tertiary amines to amine oxides, R3NO.Recommanded Product: N-tert-Butoxycarbonylhydroxylamine
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