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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260098Generated: October 30, 2026

Nitric Acid → 4-Acetamido-3-nitrobenzoic acid

https://huagongshe.com/reaction/2260098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
Reactantp-Acetamidobenzoic acidHCID 19266—
Product4-Acetamido-3-nitrobenzoic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05476849
Source datasetuspto-grants-1995_12
ORD IDord-098c92c108ca401dad6d8f53c86ce747
Source noteuspto-grants-1995_12