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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178713Generated: October 29, 2026

Methyl 2,2-difluoro-2-(fluorosulfonyl)acetate → 1-Chloro-2-fluoro-4-methoxy-3-(trifluoromethyl)benzene

https://huagongshe.com/reaction/2178713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2,2-difluoro-2-(fluorosulfonyl)acetateHCID 547667—
Reactant1-Chloro-2-fluoro-4-methoxybenzeneHCID 2724521—
Reactant1-Chloro-2-fluoro-3-iodo-4-methoxybenzeneHCID 68380100—
CatalystCopper iodideHCID 83717—
Product1-Chloro-2-fluoro-4-methoxy-3-(trifluoromethyl)benzeneHCID 68380730—

Reaction Steps

1-Chloro-2-fluoro-4-methoxybenzene was converted to 1-chloro-2-fluoro-3-iodo-4-methoxybenzene (see G. L. Grunewald et al., J. Med. Chem. 1986, 29, 1972-1982). 1-Chloro-2-fluoro-3-iodo-4-methoxybenzene was treated with methyl difluoro(fluorosulfonyl)acetate in the presence of copper iodide (A. Khilevich et al., U.S. Pat. Appl. Publ. 2010, US 20100016373) to provide 1-chloro-2-fluoro-4-methoxy-3-(trifluoromethyl)benzene. 4-Chloro-3-fluoro-2-(trifluoromethyl)phenol was then obtained by de-methylation using boron trichloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067934B2
Source datasetuspto-grants-2015_06
ORD IDord-2688e207687b4d0bb4983e61e6354074
Source noteuspto-grants-2015_06