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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500197Generated: November 2, 2026

Ethyl trifluoroacetate → 1-(3,5-Dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanone

https://huagongshe.com/reaction/1500197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trifluoroacetateHCID 9794—
Reactant1,3-Dichloro-2,4-difluoro-5-iodobenzeneHCID 87158986—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
Product1-(3,5-Dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanoneHCID 8715862569.2%

Reaction Steps

1,3-Dichloro-2,4-difluoro-5-iodobenzene (4.0 g) was dissolved in tetrahydrofuran and cooled to −10 degree. A 2.0 M solution of isopropylmagnesium chloride in tetrahydrofuran (10 ml) was added dropwise via a dropping funnel. The reaction mixture was stirred for 1 hour at same temperature. A solution of ethyl trifluoroacetate (2.76 g) in tetrahydrofuran (6 ml) was added dropwise and the reaction mixture was allowed to warm to ambient temperature. The reaction mixture was diluted with t-butyl methyl ether and washed with 1 N NaOH and then brine. The combined extracts were dried over magnesium sulfate. After filtered off, the filtrate was concentrated in vacuo to give crude product which was purified with Kugel-Rohr to give 1-(3,5-dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanone (2.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206122B2
Source datasetuspto-grants-2015_12
ORD IDord-fc999ebbfbc040319171cf64ddba7a37
Source noteuspto-grants-2015_12