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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Iodobenzoic acid | HCID 6941 | — |
| Reactant | trans-N,N'-dimethyl-1,2-cyclohexanediamine | HCID 2733821 | — |
| Reactant | HCID 178418936 | HCID 178418936 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(2H-1,2,3-Triazol-2-yl)benzoic acid | HCID 21313592 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263586B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-df79b8f20af74d3c937be0070053b970 |
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| Source note | uspto-grants-2012_09 |
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