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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291552Generated: November 1, 2026

Hydrochloric Acid → HCID 14442113, compound

https://huagongshe.com/reaction/2291552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant3-Aminobenzoic AcidHCID 7419—
Reactant2-Chlorobenzoic AcidHCID 8374—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium BromideHCID 253877—
CatalystCopperHCID 23978—
SolventMethanolHCID 887—
ProductHCID 14442113HCID 14442113—

Reaction Steps

To a 500 ml round-bottomed flask equipped with condenser and N2 inlet were added 15.7 g (0.10 mol) 2-chlorobenzoic acid, 23.3 g (0.17 mol) 3-aminobenzoic acid, 23.5 g (0.17 mol) potassium carbonate, 50 mg copper powder, and 40 ml dimethylformamide. The mixture was heated to reflux, and three 50 mg portions of methanol-washed copper(I) bromide were added. The reaction was refluxed 3.5 hours, cooled, and poured into 1 l 1N HCl. The mixture was stirred for 10 minutes, filtered, and the filtered solid washed with water, methanol, and ether, and dried to afford a gray solid, mp 277°-279° C., 19 g (73.9%). The acid was taken up in 250 ml methanol, the solution saturated with HCl and refluxed 40 hours, and cooled and evaporated. The residue was chromatographed on silica gel using methylene chloride as eluent to afford 17.46 g (61.3% overall) of a yellow oil. NMR (d, CDCl3): 3.97 (s, 3H), 6.7-8.0 (m, 8H). IR (Cm.-1, KBr): 1730 (C=0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797403
Source datasetuspto-grants-1989_01
ORD IDord-76ad14467f2e4f1c9f2c0083eb54165f
Source noteuspto-grants-1989_01