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Synlett 2013; 24(13): 1643-1648
DOI: 10.1055/s-0033-1339316
DOI: 10.1055/s-0033-1339316
letter
Rh(I)-Catalyzed Carbon–Carbon Double-Bond Formation by Coupling of (Quinolin-8-yl)methanone with Arylaldehyde Tosylhydrazone
Further Information
Publication History
Received: 11 April 2013
Accepted after revision: 05 June 2013
Publication Date:
17 July 2013 (online)
Abstract
An alternative method for the direct arylvinylation of (quinolin-8-yl)methanone with substituted N′-benzylidene-4-methylbenzenesulfonohydrazide is described. The desired 3-aryl-1-(quinolin-8-yl)prop-2-en-1-one products are obtained in high yields through the catalytic reaction of (quinolin-8-yl)methanone and N′-arylidene-4-methylbenzenesulfonohydrazide (2 equiv) with [Rh(PPh3)3Cl] (10 mol%), Ag2O (0.5 equiv), and Cs2CO3 (2 equiv) at 130 °C for 48 hours. Two plausible mechanisms involving C–H activation and migratory insertion of the carbene into the rhodium–carbon bond were proposed to explain the formation of the product.
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- 15 Synthesis of 3-Phenyl-1-(quinolin-8-yl)prop-2-en-1-one (Scheme 2 and Table 3, Entry 1); Typical Procedure: A mixture of (quinolin-8-yl)methanone (85.5 mg, 0.5 mmol), N′-benzylidene-4-methylbenzenesulfonohydrazide (548.6 mg, 1.0 mmol), Ag2O (58.0 mg, 0.25 mmol), Cs2CO3 (232 mg, 1.0 mmol), and [Rh(PPh3)3Cl] (46.65 mg, 0.05 mmol) under nitrogen in a screw-capped thick-walled Pyrex tube was heated at 130 °C with stirring. After heating for 48 h, the reaction mixture was cooled and directly purified by column chromatography on silica gel (hexane–EtOAc, 20:1) to afford 3-phenyl-1-(quinolin-8-yl)prop-2-en-1-one (75% yield).
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