Certain substituted bromobenzenes have been synthesized in acceptable yields using a novel Sandmeyer type reaction. The reactions are relatively quick and possibly proceed via a radical mechanism.

Pure 2,2'-Dibromo-9,9'-spirobifluorene was synthesized by a method that did not involve troublesome dibromination of 9,9'-spirobifluorene or Sandmeyer reaction of 2,2'-diamino-9,9'-spirobifluorene. A series of donor-acceptor orthogonally substituted 9,9'-spirobifluorene was subsequently prepared showing rich variation of fluorescence in solution and in solid state. [reaction: see text]

A novel strategy for aromatic trifluoromethylation by converting aromatic amino group into CF3 group is reported herein. This method, which can be considered as trifluoromethylation variation of the classic Sandmeyer reaction, uses readily available aromatic amines as starting materials and is performed under mild conditions.

The title compound, C12H12BrNO4S2, was obtained by the Sandmeyer reaction from ethyl 3-amino-4-cyano-5-[(2-eth-oxy-2-oxoeth-yl)sulfan-yl]thio-phene-2-carboxyl-ate. The dihedral angle between the thiophene ring and linked CO2 ester group is 2.0 (5)°.

The Sandmeyer reaction of differently C-2 substituted N-(prop-2-yn-1-ylamino)pyridines is an efficient, mild, new and practical method for the stereospecific synthesis of (E)-exo-halomethylene bicyclic pyridones bearing the imidazo[1,2-a]pyridine heterocyclic ring system.

The preparation of 5-bromo-2-naphthol (4) in three steps from 5-amino-2-naphthol (1) is described. A sulfonic acid group is introduced at the 1-position as an activating and protecting group for the Sandmeyer reaction. The sulfonate group allows for the use of only water and sulfuric acid as solvents. The sulfonic acid is introduced with three equivalents of sulfuric acid, and it is removed in ...

an efficient and environmentally benign   method for the synthesis of aryl iodides have been developed by diazotization of aromatic amines with nano2 and nanosilica periodic acid (nano-spia) as a green catalyst via grinding followed by a sandmeyer iodination by ki under solvent-free conditions at room temperature. the ensuing aryl diazonium salts supported on nano-spia were sufficiently stable ...

The title compound, C(9)H(7)IN(+)·I(3) (-)·C(4)H(8)O, was synthesized from 8-amino-quinoline using the Sandmeyer reaction. The 8-iodo-quinolinium cation is essentially planar and the triiodide ion is almost linear. N-H⋯O hydrogen bonds, and inter-molecular I⋯I [3.7100 (5) Å] and I⋯H inter-actions, between the cation, anion and solvent mol-ecules result in the formation of sheets oriented parall...

The title compound, C(9)H(7)IN(+)·Cl(-)·2H(2)O, was obtained during the synthesis of 8-iodo-quinoline from 8-amino-quinoline using the Sandmeyer reaction. The 8-iodo-quinolinium ion is almost planar. Solvent water mol-ecules and chloride ions form a hydrogen-bonded chain along the c axis via O-H⋯Cl links. The 8-iodo-quinolinium ions, which are packed along the c axis with cationic aromatic π-π ...

Arene and heteroarenediazonium o-benzenedisulfonimides can be used as efficient reagents in Sandmeyer cyanation. This work reports such reactions carried out by us under very mild conditions using tetrabutyl ammonium cyanide as a safe cyanide source and, interestingly, without the need for a Cu catalyst. The reactions have given rise to aryl nitriles in good yields (25 examples, average yield 7...