HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2,2-difluoro-2-(fluorosulfonyl)acetate → 1-Chloro-2-fluoro-4-methoxy-3-(trifluoromethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2,2-difluoro-2-(fluorosulfonyl)acetate | HCID 547667 | — |
| Reactant | 1-Chloro-2-fluoro-4-methoxybenzene | HCID 2724521 | — |
| Reactant | 1-Chloro-2-fluoro-3-iodo-4-methoxybenzene | HCID 68380100 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Product | 1-Chloro-2-fluoro-4-methoxy-3-(trifluoromethyl)benzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067934B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-2688e207687b4d0bb4983e61e6354074 |
| Source note | uspto-grants-2015_06 |