4-Nitrophenol → 1-Fluoro-2-[(4-nitrophenoxy)methyl]benzene
Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1)([O-:3])=[O:2].[F:11][C:12]1[CH:19]=[CH:18][CH:17]=[CH:16][C:13]=1[CH2:14]Br>>[F:11][C:12]1[CH:19]=[CH:18][CH:17]=[CH:16][C:13]=1[CH2:14][O:10][C:7]1[CH:8]=[CH:9][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=1Participants
3
Procedure
Prepared in analogy to example 8 from 4-nitrophenol and 2-fluoro-benzylbromide. Colorless solid. Yield=74%. MS: m/e=247.1 (M+).
Sources & evidence
- ORD record
- ord-7564f6c714bb43d8a64489a1462952cc
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07053245B2
Reaction notes
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