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2-IODO-9H-FLUOREN-9-ONE synthesis

6synthesis methods
-

Yield:3096-46-6 95%

Reaction Conditions:

with tert.-butylhydroperoxide;1-n-butyl-3-methylimidazolim bromide in water at 55; for 20 h;

Steps:

General procedure for oxygenation of benzylic C-H bonds

General procedure: Charged 0.5 mmol of 3-(9H-fluoren-2-yl)prop-2-yn-1-ol 13a (110 mg, 0.5 mmol), 0.5 mL of [bmim]Br and TBHP (0.5 mL, 3.6 mmol) were taken in a round bottom flask and heated to 55 °C until completion of the reaction. The reaction course was monitored by TLC. After completion of the reaction, the reaction mixture was extracted using ethyl acetate (3 * 4 mL). The organic layer was concentrated under vacuum and purified by column chromatography on silica gel to afford the desired product as 2-(3-hydroxyprop-1-yn-1-yl)-9H-fluoren-9-one 13b Yellow Solid;

References:

Naidu, Shivaji;Reddy, Sabbasani Rajasekhara [Journal of Molecular Liquids,2016,vol. 222,p. 441 - 445]

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