1-(4-Bromo-3-nitrophenyl)ethan-1-one → HCID 21406742, compound
Reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1I.[CH3:10][C:11]([C:13]1[CH:18]=[CH:17][C:16](Br)=[C:15]([N+:20]([O-:22])=[O:21])[CH:14]=1)=[O:12]>>[C:11]([C:13]1[CH:18]=[CH:17][C:16]([C:3]2[CH:4]=[CH:5][C:6]([F:8])=[CH:7][C:2]=2[F:1])=[C:15]([N+:20]([O-:22])=[O:21])[CH:14]=1)(=[O:12])[CH3:10]Participants
Procedure
2,4-Difluoroiodobenzene and 4-bromo-3-nitroacetophenone were reacted under Ullmann conditions to give 4-acetyl-2',4'-difluoro-2-nitrobiphenyl, b.p. 150°-158° C./0.2 mm., and this was reduced with stannous chloride to give 4-acetyl-2-amino-2',4'-difluorobiphenyl, m.p. 93°-95° C. By similar methods there were obtained 4-acetyl-2'-chloro-4'-fluoro-2-nitrobiphenyl, b.p. 178°-190°/0.2 mm m.p. 62°-64° C. and 4-acetyl-2-amino-2'-chloro-4'-fluorobiphenyl, m.p. 84°-86° C; 4-acetyl-4'-chloro-2'-fluoro-2-nitrobiphenyl, b.p. 174°-180°/0.2 mm., m.p. 85°-86° C. and 4-acetyl-2-amino-2'-fluoro-4'-chlorobiphenyl, m.p. 115° C; 4-acetyl-2',4'-dichloro-2-nitrobiphenyl, m.p. 72°-74° C. and 4-acetyl-2-amino-2',4'-dichlorobiphenyl, m.p. 75°-76° C; 4-acetyl-2' ,4'-dibromo-2-nitrobiphenyl, b.p. 210° C./0.3 mm. and 4-acetyl-2-amino-2',4'-dibromobiphenyl, m.p. 107°-109° C; 4-acetyl-4'-bromo-2'-fluoro-2-nitrobiphenyl, m.p. 116°-117° C. and 4-acetyl-2-amino-4'-bromo-2'-fluorobiphenyl, m.p. 120°-121° C; 4-acetyl-2'-bromo-4'-fluoro-2-nitrobiphenyl, b.p. 188°-200° C./0.3 mm., m.p. 75°-77° C. and 4-acetyl-2-amino-2'-bromo-4'-fluorobiphenyl, m.p. 98°-100° C; 4-acetyl-4'-bromo-2'-chloro-2-nitrobiphenyl, b.p. 185°-190° C./0.2 mm. and 4-acetyl-2-amino-4'-bromo-2'-chlorobiphenyl, m.p. 93°-95° C; and 4-acetyl-2'-bromo-4'-chloro-2-nitrobiphenyl, m.p. 84°-86° C; and 4-acetyl-2-amino-2'-bromo-4'-chlorobiphenyl, m.p. 98°-100° C.
Sources & evidence
- ORD record
- ord-0d961d84adf14bed9755a4e9908c3915
- Source dataset
- uspto-grants-1977_10
- Patent number
- US04052514
Reaction notes
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