Category: 66416-72-6

Some common heterocyclic compound, 66416-72-6, name is 4-Bromo-2-iodoaniline, molecular formula is C6H5BrIN, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. HPLC of Formula: C6H5BrIN

tert-Butyl nitrite (3 ml, 25 mmol) is added to a suspension of copper(ll) chloride (2.71 g, 20 mmol) in acetonitrile (60 ml) and the mixture is heated with stirring to 60 0C. A solution of 4- bromo-2-iodoaniline (5 g, 17 mmol) in acetonitrile (15 ml) is added dropwise, and once the addition is complete the mixture is stirred at 60 0C for 2.5 hours. The mixture is cooled to room temperature, poured into 20% aqueous hydrochloric acid and extracted with diethyl ether. The organic extract is dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated in vacuo. The residue is further purified by column chromatography on silica gel to give 4-bromo-1-chloro-2-iodobenzene (4.32 g) as an oil.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 66416-72-6, its application will become more common.

Reference:
Patent; SYNGENTA PARTICIPATIONS AG; SYNGENTA LIMITED; WO2008/71405; (2008); A1;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 66416-72-6, name is 4-Bromo-2-iodoaniline, This compound has unique chemical properties. The synthetic route is as follows., Recommanded Product: 66416-72-6

Example 187 6-(5-Bromo-2-chloro-phenyl)-N*4*-(4-chloro-phenyl)-pyrimidine-2,4-diamine To a stirred suspension of copper (II) chloride (1.62 g, 12.0 mmol) and tert-butyl nitrite (15.0 mmol) in acetonitrile (40 ml), heated at 60 C., was added a solution of 4-bromo-2-iodo-phenylamine (2.98 g, 10.0 mmol) in acetonitrile (10 ml) dropwise over 50 minutes. After stirring at 60 C. for 1 hour, the mixture was poured into 20% hydrochloric acid (200 ml) and extracted with ether (2*30 ml). The crude product was purified by flash chromatography on silica gel eluding with hexane to provide 4-bromo-1-chloro-2-iodo-benzene (2.4 g, 76% yield).

According to the analysis of related databases, 66416-72-6, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Cell Therapeutics, Inc.; US2004/204386; (2004); A1;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Some common heterocyclic compound, 66416-72-6, name is 4-Bromo-2-iodoaniline, molecular formula is C6H5BrIN, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. 66416-72-6

Step 1 : Preparation of 4-bromo-1-chloro-2-iodobenzeneterf-Butyl nitrite (11.1 ml, 93.3 mmol) is added to a suspension of copper(ll) chloride (10.04 g, 75 mmol) in acetonitrile (224 ml) and the mixture is heated with stirring to 60 0C. A solution of 4- bromo-2-iodoaniline (18.54 g, 62 mmol) in acetonitrile (56 ml) is added dropwise over about an hour, and once the addition is complete the mixture is stirred at 60 0C for 2 hours. The mixture is cooled to room temperature, poured into 20% aqueous hydrochloric acid (1.3 litres) and extracted with diethyl ether (1.5 litres). The organic extract is separated and the aqueous re- extracted with ether (1 litre). The organic extracts are combined and dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated in vacuo. The residue is further purified by column chromatography on silica gel to give 4-bromo-1-chloro-2-iodobenzene (8.62 g) as an oil.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 66416-72-6, its application will become more common.

Reference:
Patent; SYNGENTA LIMITED; WO2008/145336; (2008); A1;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com