HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401721Generated: October 28, 2026
Ethyl trifluoroacetate → 1-(4-Chloro-2-fluorophenyl)-2,2,2-trifluoroethan-1-one
https://huagongshe.com/reaction/401721
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 4-Chloro-2-fluoro-1-iodobenzene | HCID 2736562 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Chloro-2-fluorophenyl)-2,2,2-trifluoroethan-1-one | HCID 24726836 | — |
Reaction Steps
To a solution of n-BuLi (1.6 M in hexanes, 4.68 mmol, 2.93 mL) in dry THF was slowly added 4-chloro-2-fluoro-1-iodo-benzene 67h (3.9 mmol, 1.0 g) at −78° C. under N2. The mixture was stirred for 1 h at −78° C. and ethyl trifluoroacetate 67b (0.51 mL, 4.29 mmol) was added. The reaction was allowed to warm to room temperature overnight and was quenched with saturated aqueous NH4Cl solution. The mixture was extracted with EtOAc. The organic extracts were concentrated and purified by flash column chromatography (silica gel, 15% EtOAc/hexanes) to give compound 67i.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741887B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-cf3f170aeee44278a87fe18e9d49c742 |
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| Source note | uspto-grants-2014_06 |
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