1970
DOI: 10.3329/bjsir.v42i1.354
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and Correlation of Spectral Properties of Some Substituted 1,3-Diphenyl-2-Propen-1-Ones

Abstract: Seven arylideneacetophenones: 1-(4-chlorophenyl)-3-phenyl-2-propen-1-one (1a), 1-(4-nitrophenyl)-3-phenyl-2-propen-1-one (1b) , 1-(4-methoxyphenyl)-3-phenyl-2- propen-1-one (1c) , 1-(4-methylphenyl)-3-phenyl-2-propen-1-one (1d) , 1-(4- chlorophenyl)-3-(4-methoxyphenyl)-2-propen-1-one (1e) , 1-(4-methylphenyl)-3-(4- methoxyphenyl)-2-propen-1-one (1f) and 1,3-di(4-methoxyphenyl)-2-propen-1-one (1g) were synthesized from the corresponding substituted acetophenones and benzaldehydes in presence of sodium hydroxi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
4
0

Year Published

2011
2011
2023
2023

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 10 publications
(5 citation statements)
references
References 11 publications
(9 reference statements)
0
4
0
Order By: Relevance
“…Cations are moved further away a Yield of the isolated condensation reaction product containing ≥ 99.0% of the base stock (by GC-MS) using the molar ratio benzaldehyde: ethyl cyanoacetate (acetophenone): ionic liquid = 1:1:2. b Yield of the product using glycine as a catalyst and the molar ratio benzaldehyde: ethyl cyanoacetate: ionic liquid: glycine = 1:1:2:1. c Yield in ethanol in the presence of glycine as a catalyst according to a described [15] procedure. d Yield in a 1:1 water/ethanol mixture in the presence of NaOH as a catalyst according to a described [16] procedure.…”
Section: Resultsmentioning
confidence: 99%
“…Cations are moved further away a Yield of the isolated condensation reaction product containing ≥ 99.0% of the base stock (by GC-MS) using the molar ratio benzaldehyde: ethyl cyanoacetate (acetophenone): ionic liquid = 1:1:2. b Yield of the product using glycine as a catalyst and the molar ratio benzaldehyde: ethyl cyanoacetate: ionic liquid: glycine = 1:1:2:1. c Yield in ethanol in the presence of glycine as a catalyst according to a described [15] procedure. d Yield in a 1:1 water/ethanol mixture in the presence of NaOH as a catalyst according to a described [16] procedure.…”
Section: Resultsmentioning
confidence: 99%
“…Chalcones were synthesized by the base‐catalyzed Claisen–Schmidt condensation reaction of appropriately substituted acetophenones and aldehydes as described in the literature …”
Section: Methodsmentioning
confidence: 99%
“…1-Uncorrected melting points were measured by digital MP 161 MSRS melting point apparatus General Procedure Chalcones were synthesized by base catalyzed Claisen-Schmidt condensation reaction of acetophenone and aldehyde by known literature method [38,39].…”
Section: Experimental A-techniquesmentioning
confidence: 99%