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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869022Generated: October 27, 2026

Cesium carbonate → 3-fluoro-2-(1H-1,2,3-triazol-1-yl)benzoic acid

https://huagongshe.com/reaction/869022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1H-1,2,3-TriazoleHCID 67516—
Reactant(1R,2R)-N1,N1-Dimethylcyclohexane-1,2-diamineHCID 11275066—
Reactant3-Fluoro-2-iodobenzoic acidHCID 22320308—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-fluoro-2-(1H-1,2,3-triazol-1-yl)benzoic acidHCID 67087111—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 3-fluoro-2-iodobenzoic acid (4.5 g, 16.9 mmol) dissolved in dioxane (33.8 mL) and H2O (0.09 mL) was added Cs2CO3 (11.02 g, 33.8 mmol), CuI (161 mg, 0.85 mmol), 2H-1,2,3-triazole (1.96 mL, 33.8 mmol), and trans-N,N-dimethyl-1,2-cyclohexanediamine (0.53 mL, 3.38 mmol). The mixture was then heated to 100° C. overnight, cooled to room temperature, diluted with H2O, and extracted with EtOAc. The aqueous layer was then acidified and extracted with EtOAc. The combined organics were dried and concentrated. From this concentrate a solid precipitated to provide intermediate A-33 (285 mg, 8%). MS (ESI) mass calcd for C9H6FN3O2, 207.0. m/z found 208.1 [M+H]+. 1H NMR (500 MHz, Methanol-d4) δ 6.81-6.77 (m, 1H), 6.46-6.40 (m, 2H), 6.30-6.23 (m, 1H), 6.18-6.12 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969352B2
Source datasetuspto-grants-2015_03
ORD IDord-9bef943801574c0c9548f24bf3b6d421
Source noteuspto-grants-2015_03