2006
DOI: 10.1107/s1600536806044588
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Ethyl 2-acetyl-3-anilinobutanoate

Abstract: Key indicatorsSingle-crystal X-ray study T = 295 K Mean (C-C) = 0.004 Å R factor = 0.052 wR factor = 0.135 Data-to-parameter ratio = 16.1For details of how these key indicators were automatically derived from the article, see

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Cited by 3 publications
(4 citation statements)
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“…Our group reported the catalyst‐free synthesis of alkyl 2‐acetyl‐3‐(phenylamino)butanoates using arylamines, acetaldehyde and β‐ketoesters [19–21] . The amine and acetaldehyde initially react to give an imine, which in turn reacts with a β‐ketoester through a Michael addition.…”
Section: Resultsmentioning
confidence: 99%
“…Our group reported the catalyst‐free synthesis of alkyl 2‐acetyl‐3‐(phenylamino)butanoates using arylamines, acetaldehyde and β‐ketoesters [19–21] . The amine and acetaldehyde initially react to give an imine, which in turn reacts with a β‐ketoester through a Michael addition.…”
Section: Resultsmentioning
confidence: 99%
“…For related structures see: Rajesh et al (2009); Priya et al (2006). For hydrogen-bond motifs, see: Bernstein et al (1995).…”
Section: Related Literaturementioning
confidence: 99%
“…For the crystal structure of ethyl 2-acetyl-3-anilinobutanoate, see: Priya et al (2006). For hydrogen-bond motifs, see: Bernstein et al (1995).…”
Section: Related Literaturementioning
confidence: 99%
“…Ethyl butanoate is commonly used as an artificial flavoring agent in alcoholic beverages, perfumery products and as a plasticizer for cellulose. The crystal structure of ethyl 2-acetyl-3-anilinobutanoate has been reported (Priya et al, 2006).…”
Section: Data Collectionmentioning
confidence: 99%