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HERO ID
5345750
Reference Type
Journal Article
Title
SYNTHESIS OF 2,4-DIFLUOROANILINE AND 1,3-DIFLUOROBENZENE FROM 1,2,4-TRICHLORBENZENE
Author(s)
Mason, J; Milner, DJ
Year
1994
Is Peer Reviewed?
1
Journal
Synthetic Communications
ISSN:
0039-7911
Volume
24
Issue
4
Page Numbers
529-532
Language
English
DOI
10.1080/00397919408011503
Web of Science Id
WOS:A1994MZ36900012
Abstract
Nitration of inexpensive 1,2,4-trichlorobenzene gave 2,4,5-trichloronitrobenzene (90%) which was treated with KF to form 2,4-difluoro-5-chloronitrobenzene (70%). This was selectively hydrogenated over Pd / C to give 2,4-difluoroaniline (80%). Deamination afforded 1,3-difluorobenzene. The sequence avoids the need for costly 1,3-dichlorobenzene.
Keywords
1,3 difluorobenzene; 2,4 difluoroaniline; organofluorine derivative; unclassified drug; article; reaction analysis; synthesis
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