Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

1H-Benzimidazol-2-amine,5-chloro-1-methyl-(9CI) synthesis

5synthesis methods
55305-43-6 Synthesis
N-Cyano-N-phenyl-p-toluenesulfonaMide

55305-43-6
65 suppliers
$23.00/100mg

59681-66-2 Synthesis
4-Chloro-N1-methylbenzene-1,2-diamine

59681-66-2
56 suppliers
$52.00/100mg

1H-Benzimidazol-2-amine,5-chloro-1-methyl-(9CI)

103748-25-0
16 suppliers
inquiry

-

Yield:103748-25-0 86%

Reaction Conditions:

with lithium hexamethyldisilazane in tetrahydrofuran;hexane at 5 - 20; for 1 h;Green chemistry;

Steps:

Typical Experimental Procedure for the Synthesis of 2-Aminobenzaxozole from o-Aminophenol

General procedure: To a solution of o-aminophenol (400 mg, 3.67 mmol) and NCTS (998 mg, 3.67 mmol) in THF (6 mL), 1 M LiHMDS in hexane (3.67 mL, 3.67 mmol) was added and stirred at 5 °C to r.t. for 1h. Then the reaction mixture was poured in ice water and stirred for 15 min. Then extracted with EtOAc, the organic layer was separated. The organic layer was washed with brine solution.Then organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to obtained pure 2-aminobenzaxozole in 90% yield (471 mg).

References:

Kasthuri, Mahesh;Babu, H. Sharath;Kumar, K. Shiva;Sudhakar, Ch.;Kumar, P. V. Nagendra [Synlett,2015,vol. 26,# 7,art. no. ST-2014-B0948-L,p. 897 - 900]

1H-Benzimidazol-2-amine,5-chloro-1-methyl-(9CI) Related Search: