PENGARUH GUGUS NITRO TERHADAP WAKTU SINTESIS 2,3 DIFENILKUINAZOLIN-4(3H)-ON 3-(4-NITROFENIL)-2-FENILKUINAZOLIN-4(3H)-ON DENGAN BANTUAN IRADIASI GELOMBANG MIKRO
This study aims to synthesize between 3-(4-nitrophenyl)-2- phenylquinazolin-4(3H)-on and 2,3-diphenylquinazolin-4(3H)-one The reaction between 2-phnyl-4H-benzo[d][1,3]oxazin-4-one with aniline gave 3-(4-nitrophenyl)-2-phenylquinazolin-4(3H)-one, while the reaction between 4- hydroxybenzohyd2-phe...
Saved in:
Main Author: | |
---|---|
Format: | Theses and Dissertations NonPeerReviewed |
Language: | Indonesian Indonesian |
Published: |
2017
|
Subjects: | |
Online Access: | http://repository.unair.ac.id/65247/1/FF.KF.23.17%20.%20Pur.p%20-%20ABSTRAK.pdf http://repository.unair.ac.id/65247/2/FF.KF.23.17%20.%20Pur.p%20-%20SEC.pdf http://repository.unair.ac.id/65247/ http://lib.unair.ac.id |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Universitas Airlangga |
Language: | Indonesian Indonesian |
Summary: | This study aims to synthesize between 3-(4-nitrophenyl)-2-
phenylquinazolin-4(3H)-on and 2,3-diphenylquinazolin-4(3H)-one
The reaction between 2-phnyl-4H-benzo[d][1,3]oxazin-4-one with
aniline gave 3-(4-nitrophenyl)-2-phenylquinazolin-4(3H)-one, while
the reaction between 4- hydroxybenzohyd2-phenyl-4Hbenzo[
d][1,3]oxazin-4-one and p-nitroaniline gave 3-(4-2,3-
diphenylquinazolin-4(3H)-one,. The synthesize were completed by
microwave irradiation N-phenyl-2-benzamidobenzamide was
obtained as amorphous, lightweight, and white crystal with 96%
percentage yield and 20 minutes reaction, while 3-(4-nitrophenyl)-2-
phenylquinazolin-4(3H)-one,was obtained as lightweight and
colorless needles with 58% percentage yield and 30 minutes s. The
structure of resulted compound were confirmed by UV- Vis
spectrophotometer, IR spectrophotometer and 1H-NMR
spectrometer. It was concluded that nitro group responsible to
increase time of completing reaction in the synthesize of 23-(4-
nitrophenyl)-2-phenylquinazolin-4(3H)-one. The time of completing
reaction 3-(4-nitrophenyl)-2-phenylquinazolin-4(3H)-one was higher
than the time of completing reaction of N-phenyl-2-
benzamidobenzamide |
---|