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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382579Generated: October 30, 2026

2-Iodobenzoic acid → 2-(2H-1,2,3-Triazol-2-yl)benzoic acid

https://huagongshe.com/reaction/2382579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Iodobenzoic acidHCID 6941—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
ReactantHCID 178418936HCID 178418936—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(2H-1,2,3-Triazol-2-yl)benzoic acidHCID 21313592—

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of 2-iodobenzoic acid (3.0 g, 12.09 mmol) in DMF was treated with (1.5 g, 21.7 mmol) 1,2,3-triazole, 7.08 g (21.7 mmol) CsCO3, 114 mg (0.60 mmol) CuI and 310 mg (2.17 mmol) trans-N,N′-dimethylcyclohexane-1,2-diamine. The mixture was heated at 120° C. for 10 min in a microwave reactor. The reaction was cooled to rt, diluted with EtOAc, and filtered through Celite. The residue was purified by gradient elution on SiO2 (0 to 10% MeOH in DCM with 0.1% AcOH) to give the faster eluting desired 2-(2H-1,2,3-triazol-2-yl)benzoyl acid, B-1. Data for B-1: 1HNMR (500 MHz, DMSO-d6) δ 13.05 (br s, 1H), 8.12 (s, 2H), 7.81-7.52 (m, 4H) ppm. The undesired 2-(1H-1,2,3-triazol-2-yl)benzoic acid (B-2) eluted second.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263586B2
Source datasetuspto-grants-2012_09
ORD IDord-df79b8f20af74d3c937be0070053b970
Source noteuspto-grants-2012_09