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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430032Generated: October 31, 2026

Benzoic Acid → N-(2-aminophenyl)benzamide

https://huagongshe.com/reaction/430032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantTrifluoroacetic acidHCID 6422—
ReactantO-PhenylenediamineHCID 7243—
SolventDimethyl SulfoxideHCID 679—
ProductN-(2-aminophenyl)benzamideHCID 75940859.8%

Reaction Steps

1.62 g (10 mmole) of N,N′-carbonyldiimidazole were added to a dimethyl sulfoxide (10 ml) solution including 1.12 g (10 mmole) of benzoic acid, followed by stirring at room temperature for 1 hour. After the addition of 2.16 g (20 mmole, 2 equivalents) of 1,2-phenylenediamine, 1.9 ml of trifluoroacetic acid were added dropwise at room temperature. After reaction had been further carried out at room temperature for 15 hours, a post-treatment was performed in the same manner as in Example 6 to obtain 1.27 g (yield: 59%) of N-(2-aminophenyl)benzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06320078B1
Source datasetuspto-grants-2001_11
ORD IDord-18f931a5b2e64e3eba60a5611f30c625
Source noteuspto-grants-2001_11