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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339127Generated: October 25, 2026

Benzene, 1-iodo-3-(trifluoromethyl)- → 2,2-Difluoro-1-[3-(trifluoromethyl)phenyl]-1-propanone

https://huagongshe.com/reaction/339127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-iodo-3-(trifluoromethyl)-HCID 67868—
Reactant2,2-difluoro-N-methoxy-N-methylpropanamideHCID 58736313—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product2,2-Difluoro-1-[3-(trifluoromethyl)phenyl]-1-propanoneHCID 58247996—

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution of 2-propylmagnesium chloride in THF (1.3 M, 7.5 ml) was cooled to −15° C. and admixed with 1-iodo-3-(trifluoromethyl)benzene (2.80 g, 10.2 mmol). The reaction mixture was stirred at −15° C. for 1 h, warmed to room temperature and admixed dropwise with a solution of 2,2-difluoro-N-methoxy-N-methylpropanamide (1.43 g, 9.35 mmol; prepared according to Synth. Comm. 2008 (38), 1940-1945), and stirred at room temperature overnight. Then the mixture was added to ice-cold dilute hydrochloric acid and extracted with ethyl acetate. The combined organic phases were dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by means of silica gel chromatography with the eluent cyclohexane/ethyl acetate (EA) (0% EA to 30% EA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889878B2
Source datasetuspto-grants-2014_11
ORD IDord-dcbaa6e30ea6492190224c0783530890
Source noteuspto-grants-2014_11