Nitrofungin → 2-Chloro-1-(3-fluoro-benzyloxy)-4-nitro-benzene
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[OH:11].[F:12][C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=1)[CH2:16]Br>>[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[O:11][CH2:16][C:15]1[CH:18]=[CH:19][CH:20]=[C:13]([F:12])[CH:14]=1Participants
3
Procedure
Prepared in analogy to example 8 from 2-chloro-4-nitrophenol and 3-fluoro-benzylbromide. Colorless solid. Yield=84%. MS: m/e=281.0 (M+).
Sources & evidence
- ORD record
- ord-5bdf6155f3e44c998bdaccdf478e9f55
- Source dataset
- uspto-grants-2004_07
- Patent number
- US06762320B2
Reaction notes
Loading…