2-Nitrophenol → 1-[2-(2-Chloroethoxy)ethoxy]-2-nitrobenzene
Reaction equation
CO[C:3]1[CH:4]=[CH:5][C:6]([N+:16]([O-:18])=[O:17])=[C:7]([O:9][CH2:10][CH2:11][O:12][CH2:13][CH2:14][Cl:15])[CH:8]=1.[Na].[N+](C1C=CC=CC=1O)([O-])=O.COC1C=CC([N+]([O-])=O)=C(O)C=1>>[N+:16]([C:6]1[CH:5]=[CH:4][CH:3]=[CH:8][C:7]=1[O:9][CH2:10][CH2:11][O:12][CH2:13][CH2:14][Cl:15])([O-:18])=[O:17]Participants
5
Procedure
This compound was prepared in a manner analogous to the preparation of 5-methoxy-2-nitro-[2-(2-chloroethoxy)ethoxy]benzene for crown ether XIX, except that the sodium salt of o-nitrophenol was used instead of the sodium salt of 5-methoxy-2-nitrophenol.
Sources & evidence
- ORD record
- ord-e0dfb138865d4946b8ff19d28c2d5609
- Source dataset
- uspto-grants-1985_03
- Patent number
- US04504368
Reaction notes
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