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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207566Generated: October 23, 2026

2,2-Difluoro-2-(fluorosulfonyl)acetic acid → Ethyl 6-difluoromethoxymethylpyridine-2-carboxylate

https://huagongshe.com/en/reaction/2207566

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Difluoro-2-(fluorosulfonyl)acetic acidHCID 2737516—
Reactant2-Pyridinecarboxylic acid, 6-(hydroxymethyl)-, ethyl esterHCID 10921141—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventAcetonitrileHCID 6342—
ProductEthyl 6-difluoromethoxymethylpyridine-2-carboxylateHCID 6671837213%

Reaction Steps

2,2-Difluoro-2-(fluorosulfonyl)acetic acid (495 mL, 4.79 mmol) was added dropwise to a solution of ethyl 6-hydroxymethylpyridine-2-carboxylate (800 mg, 4.79 mmol) and CuI (91 mg, 0.479 mmol) in MeCN (10 mL) at room temperature at a rate to maintain the internal temperature <30° C. The mixture was stirred for a further 20 min at room temperature, poured onto brine/water and extracted with EtOAc (×3). The combined extracts were dried (MgSO4), filtered, evaporated and purified by column chromatography (4:1 to 2:1, isohexane:EtOAc) to give the title compound (130 mg, 13%) as a colorless oil; NMR δH (400 MHz, CDCl3) 8.01 (1H, d, J 7.5 Hz), 7.89 (1H, t, J 7.5 Hz), 7.66 (1H, d, J 7.5 Hz), 6.41 (1H, t, J 74.0 Hz), 5.14 (2H, s), 4.49 (2H, q, J 7.0 Hz), 1.44 (3H, t, J 7.0H); (M+H)+ 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376443B2
Source datasetuspto-grants-2016_06
ORD IDord-2d1c22284e88425181549ff89db4af20
Source noteuspto-grants-2016_06