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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 1,3-Dichloro-2,4-difluoro-5-iodobenzene | HCID 87158986 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 1-(3,5-Dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanone | HCID 87158625 | 69.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09206122B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-fc999ebbfbc040319171cf64ddba7a37 |
|---|
| Source note | uspto-grants-2015_12 |
|---|