Thionyl Chloride → 2-Amino-3-nitrobenzoyl chloride
Reaction equation
[NH2:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:16])=O>>[NH2:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([Cl:16])=[O:5]Participants
3
Procedure
A mixture of 9.90 parts of 2-amino-3-nitrobenzoic acid and 32.4 parts of thionyl chloride was stirred for 15 min at reflux temperature under argon. The excess of thionyl chloride was evaporated, yielding 10.8 parts (100%) of 2-amino-3-nitrobenzoyl chloride (interm. 39).
Workup
- temperatureat reflux temperature under argon
- customThe excess of thionyl chloride was evaporated
Sources & evidence
- ORD record
- ord-2efa173836474511a5a4f86436526802
- Source dataset
- uspto-grants-1993_12
- Patent number
- US05270464
Reaction notes
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