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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425475Generated: November 1, 2026

2,2-Difluoro-2-(fluorosulfonyl)acetic acid → methyl 3-[(2S)-1-(difluoromethoxy)propan-2-yl]oxy-5-phenylmethoxy-benzoate

https://huagongshe.com/reaction/2425475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Difluoro-2-(fluorosulfonyl)acetic acidHCID 2737516—
Reactantmethyl 3-[(2S)-1-hydroxypropan-2-yl]oxy-5-phenylmethoxy-benzoateHCID 59127113—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventAcetonitrileHCID 6342—
Productmethyl 3-[(2S)-1-(difluoromethoxy)propan-2-yl]oxy-5-phenylmethoxy-benzoateHCID 59127143—

Reaction Conditions

Temperature45 °C

Reaction Steps

2,2-Difluoro-2-fluorosulfonyl-acetic acid (CAS no. 1717-59-5) (0.239 mL, 2.31 mmol) was added dropwise, with stirring, to a degassed mixture of methyl 3-[(2S)-1-hydroxypropan-2-yl]oxy-5-phenylmethoxy-benzoate (0.73 g, 2.31 mmol) and copper (I) iodide (88 mg, 0.46 mmol) in acetonitrile (10 mL) at 45° C. The reaction was stirred at 45° C. for 24 hours. The solvent was removed in vacuo and ethyl acetate (30 mL) added. The organics were washed with water (30 mL), brine (30 mL), dried (MgSO4), filtered and the solvent removed in vacuo. The residue was chromatographed on silica, eluting with a gradient of 0-30% ethyl acetate in isohexane, to give the desired compound (0.11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964725B2
Source datasetuspto-grants-2011_06
ORD IDord-5e220bcbc9dc48ceafb6f6d0d4d45bef
Source noteuspto-grants-2011_06