4-Nitro-o-anisic acid → HCID 18465928, compound
Reaction equation
[N+:1]([CH2:3][C:4]([O:6][CH3:7])=[O:5])#[C-:2].[CH3:8][O:9][C:10]1[CH:18]=[C:17]([N+:19]([O-:21])=[O:20])[CH:16]=[CH:15][C:11]=1[C:12](O)=[O:13]>>[CH3:8][O:9][C:10]1[CH:18]=[C:17]([N+:19]([O-:21])=[O:20])[CH:16]=[CH:15][C:11]=1[C:12]1[O:13][CH:2]=[N:1][C:3]=1[C:4]([O:6][CH3:7])=[O:5]Participants
3
Procedure
The procedures of Example 1-(1) were followed, except for replacing the ethyl isocyanoacetate with 9.9 g (0.1 mol) of methyl isocyanoacetate, to obtain 15.4 g (0.055 mol 61.5% based on the 2-methoxy-4-nitrobenzoic acid) of the title compound.
Workup
- customto obtain 15.4 g (0.055 mol 61.5%
Sources & evidence
- ORD record
- ord-a8d9477b5b5a4fa9bb7e9f7a5f246251
- Source dataset
- uspto-grants-2002_07
- Patent number
- US06423849B1
Reaction notes
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