HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 4-Acetamido-3-nitrobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | p-Acetamidobenzoic acid | HCID 19266 | — |
| Product | 4-Acetamido-3-nitrobenzoic acid | HCID 73758 | — |
Reaction Steps
In this reaction sequence, partially described by Kumar et al., J. Med. Chem., 27, pp. 1083-1089 (1984), 4-acetamidobenzoic acid is utilized as a starting material and is nitrated using, for instance, fuming nitric acid at about -10° to about 10° C. for 1-4 hours to afford 3-nitro-4-acetamidobenzoic acid. This compound is then reacted with thionyl chloride in a non-polar, aprotic solvent to afford the corresponding 3-nitro-4-acetamidobenzoyl chloride, which is then further reacted with the R'1 --H amine wherein R'1 is an amino group or a --NR4R5 group, to afford the 3-nitro-4-acetamino compound of formula V.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05476849 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-098c92c108ca401dad6d8f53c86ce747 |
| Source note | uspto-grants-1995_12 |