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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920737Generated: October 30, 2026

2,2-Difluoro-2-(fluorosulfonyl)acetic acid → Ethyl 1-((difluoromethoxy)methyl)cyclobutanecarboxylate

https://huagongshe.com/reaction/920737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Difluoro-2-(fluorosulfonyl)acetic acidHCID 2737516—
ReactantEthyl 1-(hydroxymethyl)cyclobutane-1-carboxylateHCID 15670506—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventAcetonitrileHCID 6342—
ProductEthyl 1-((difluoromethoxy)methyl)cyclobutanecarboxylateHCID 11806243776%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of ethyl 1-(hydroxymethyl)cyclobutanecarboxylate (0.2 g, 1.264 mmol) in acetonitrile (2 mL) was added CuI (0.120 g, 0.632 mmol) and the reaction mass was heated to 50° C. 2,2-Difluoro-2-(fluorosulfonyl)acetic acid (0.196 mL, 1.896 mmol) added dropwise to the solution and the reaction mixture was stirred at 50° C. for 4 h. The reaction mixture was cooled to RT and extracted with EtOAc (3×15 mL). The combined organic layer was washed with a 10% aqueous solution of NaHCO3, dried over Na2SO4, filtered and the filtrate concentrated to afford Intermediate 223A as a brown oil (0.2 g, 76%). 1H NMR (300 MHz, DMSO-d6) δ ppm 6.94-6.39 (m, 1H), 4.16-3.99 (m, 4H), 2.41-2.17 (m, 2H), 2.08-1.73 (m, 4H), 1.26-1.09 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273058B2
Source datasetuspto-grants-2016_03
ORD IDord-42822d8344754ca3be083fce78d0b132
Source noteuspto-grants-2016_03