3-methyl-4,5,6,7-tetrahydro-1-benzothiophene-2-carboxylic acid3-methyl-4 5 6,7-tetrahydro-1-benzothiophene-2-carboxylic酸.pdfVIP

3-methyl-4,5,6,7-tetrahydro-1-benzothiophene-2-carboxylic acid3-methyl-4 5 6,7-tetrahydro-1-benzothiophene-2-carboxylic酸.pdf

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3-methyl-4,5,6,7-tetrahydro-1-benzothiophene-2-carboxylic acid3-methyl-4 5 6,7-tetrahydro-1-benzothiophene-2-carboxylic酸

Molbank 2010, M648 OPEN ACCESS molbank ISSN 1422-8599 /journal/molbank Short Note 3-Methyl-4,5,6,7-tetrahydro-1-benzothiophene-2- carboxylic Acid Sembian Ruso Jayaraman 1,*, Madhavan Sridharan 1 and Rajendiran Nagappan 2 1 Syngene Intl. Ltd., Biocon Park, Plot No.23, Bommasandra IV phase, Jigani Link Road, Bangalore-560 099, India 2 Department of Polymer Chemistry, University of Madras, Gundy Campus, Chennai-600 025, India * Author to whom correspondence should be addressed; E-Mail: Sembian.Ruso@; Tel.: +919880455664, 9180 2808 2808. Received: 01 December 2009 / Accepted: 24 December 2009 / Published: 6 January 2010 Abstract: 3-Methyl-4,5,6,7-tetrahydro-1-benzothiophene-2-carboxylic acid was synthesized chemoselectively from 3-formyl-4,5,6,7-tetrahydro-1-benzothiophene-2- carboxylic acid, using Et SiH/I as a reducing agent. The title compound was characterized 3 2 1 NMR, 13C NMR and LCMS. by IR, H Keywords: triethylsilane; iodine; 3-formyl-4,5,6,7-tetrahydro-1-benzothiophene 1. Introduction In recent years, the popularity and usage of silicon reagents have tremendously increased due to their stereoselectivity [1] and chemoselectivity [2]. The reductive halogenations of carbonyl compounds were promoted by silic

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