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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623715Generated: October 25, 2026

Iodine → 4-[[5-ethoxy-2-(4-fluorophenyl)-2H-1,2,3-triazol-4-yl]methyl]-2-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/623715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantPhosphinic AcidHCID 4124402—
Reactant[5-ethoxy-2-(4-fluorophenyl)-2H-1,2,3-triazol-4-yl][2-(trifluoromethyl)-4-pyridinyl]methanoneHCID 90109653—
SolventAcetic AcidHCID 176—
Product4-[[5-ethoxy-2-(4-fluorophenyl)-2H-1,2,3-triazol-4-yl]methyl]-2-(trifluoromethyl)pyridineHCID 90111713—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of [5-ethoxy-2-(4-fluorophenyl)-2H-1,2,3-triazol-4-yl][2-(trifluoromethyl)-4-pyridinyl]methanone (i.e. the product of Step C, 2.7 g, 7.1 mmol) in acetic acid (15 mL) was added iodine (1.8 g, 7.1 mmol) and hypophosphorous acid (50% in water, 3.1 mL, 28.4 mmol). The mixture was heated to 110° C. under a nitrogen atmosphere for 6 h. The reaction mixture was cooled to 23° C. and neutralized to ˜pH 7 with 1 M NaOH and a saturated aqueous sodium bicarbonate solution. The mixture was extracted with ethyl acetate (2×15 mL), dried (MgSO4) and concentrated under reduced pressure. The crude residue was purified by chromatography on silica gel eluting with 0 to 20% ethyl acetate in hexanes to afford the title compound (2.1 g) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302999B2
Source datasetuspto-grants-2016_04
ORD IDord-637180d00d444c1e88d1d15f9f75df97
Source noteuspto-grants-2016_04