Nitric Acid → HCID 15125648, compound
Reaction equation
[N+:1]([O-:4])(O)=[O:2].OS(O)(=O)=O.C([O:13][C:14]1[CH:23]=[C:22]([NH:24][C:25](=[O:27])[CH3:26])[C:21]([Cl:28])=[CH:20][C:15]=1[C:16]([O:18][CH3:19])=[O:17])(=O)C>>[N+:1]([C:23]1[C:22]([NH:24][C:25](=[O:27])[CH3:26])=[C:21]([Cl:28])[CH:20]=[C:15]([C:16]([O:18][CH3:19])=[O:17])[C:14]=1[OH:13])([O-:4])=[O:2]Participants
4
Conditions
- Temperature
- -10 °C
Procedure
To a mixture of 90 ml concentrated HNO3 and 10 ml concentrated H2SO4 cooled to -10° C. is added portionwise over 5 minutes 10.9 g (38.2 mmol) methyl 2-acetoxy-4-acetylamino-5-chlorobenzoate. The mixture is stirred another 5 minutes and poured into ice water (400 ml). The ppt. which forms is filtered, washed (H2O) and dried to obtain methyl 3-nitro-4-acetylamino-5-chlorosalicylate; m.p. 166°-69° C.
Workup
- filtrationwhich forms is filtered
- washwashed (H2O)
- customdried
Sources & evidence
- ORD record
- ord-bc62d50c8f89450a8e013fd882be5e8b
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04935511
Reaction notes
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