Next Article in Journal
Synthesis of rac-tert-butyl 3-(benzyloxycarbonylamino)-2-(4-bromophenyl)-tetrahydrofuran-3-carboxylate
Previous Article in Journal
Synthesis of (2R,3S)-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl) 2-(4-bromophenyl)-3-(tert-butoxy-carbonylamino)-tetrahydrofuran-3-carboxylate and (2S,3R)-((1R,2S,5R)-2-isopropyl- 5-methylcyclohexyl)2-(4- bromophenyl)-3-(tert-butoxy¬carbonyl¬amino)-tetrahydrofuran-3-carboxylate
Molbank 2009, 2009(1), M595; doi:10.3390/M595
Short Note

Synthesis of 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea

,  and *
Received: 7 January 2009 / Accepted: 13 March 2009 / Published: 18 March 2009
Download PDF [155 KB, uploaded 18 March 2009]

Abstract

An unexpected product, 1-[(2-oxonaphthalen-1(2H)-ylidene)methyl]urea 4 of the condensation reaction of 2-hydroxy-1-naphthaldehyde with or without ethyl benzoylacetate and urea under hydrochloric acid-catalyzed and solvent-free conditions is reported.
Keywords: 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea; Condensation reaction Solvent-free conditions 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea; Condensation reaction Solvent-free conditions
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Supplements

Share & Cite This Article

Further Mendeley | CiteULike
Export to BibTeX |
EndNote
MDPI and ACS Style

Xu, J.; Chen, A.; Liu, Q. Synthesis of 1-[(2-Oxonaphthalen-1(2H)-ylidene)methyl]urea. Molbank 2009, 2009, M595.

View more citation formats

Article Metrics

Comments

Citing Articles

[Return to top]
Molbank EISSN 1422-8599 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert