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233-34-1

1H-BENZO(G)INDOLE synthesis

10synthesis methods
-

Yield:233-34-1 97%

Reaction Conditions:

with platinum on alumina;zinc oxide at 185; for 24 h;Sealed tube;regioselective reaction;

Steps:

General Procedure A: Ethylene Glycol as Solvent

General procedure: The starting material (1-aminonaphthalene (1a), 2-aminonaphthalene (1b), 1-aminoanthracene (2a), or 2-aminoanthracene (2b)) (2 mmol), Pt/Al2O3 (132 mg, 1.7 mol%), ZnO dispersion (22 μL, 4.5 mol%), and ethylene glycol (5 mL) were mixed in a 50 mL glass reaction tube. The tube was sealed and put into a reaction station with stirring at 185 °C for 24 h. The reaction mixture was cooled to room temperature. A volume of 10 mL of ethyl acetate was added, and the crude mixture was filtered through a 0.2 m PTFE filter. The reaction mixture was extracted with brine (3 × 20 mL), and the organic layer was dried with Na2SO4, filtered, and concentrated under vacuum. The residue was purified, when required, by column chromatography on silica gel with hexane/ethyl acetate mixtures. The isolated compounds are described in order of elution.

References:

Gonzalez-Sanchis, Nerea;Perez-Quilez, Paula;Bellezza, Delia;Flor-Sanchez, Anna;Ballesteros, Rafael;Ballesteros-Garrido, Rafael [Synthesis,2022,vol. 54,# 23,p. 5226 - 5232]

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