HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930415Generated: November 1, 2026
Ethyl fluoroacetate → HCID 86732254, compound
https://huagongshe.com/reaction/930415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl fluoroacetate | HCID 9988 | — |
| Reactant | 3-Bromo-2-fluorotoluene | HCID 108855 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86732254 | HCID 86732254 | 80% |
Reaction Steps
A solution of 1-bromo-2-fluoro-3-methylbenzene (7.0 g, 37.0 mmol) in THF (60 mL) was brought to −78° C. followed by the dropwise addition of butyllithium (15.55 ml, 38.9 mmol). The resulting mixture was stirred at −78° C. for 1 h then neat ethyl 2-fluoroacetate (3.76 ml, 38.9 mmol) was added dropwise. After 30 min the reaction went to completion. The reaction was quenched at −78° C. with saturated NH4Cl, warmed to rt and transferred to a separatory funnel. The aqueous phase was extracted with EtOAc and the combined organic extracts were washed with brine, dried over Na2SO4, filtered, concentrated and chromatographed on silica gel using 0-10% EtOAc/hexanes to afford a colorless oil that turned into a white solid as 2-fluoro-1-(2-fluoro-3-methylphenyl)ethanone (5.03 g, 29.6 mmol, 80% yield). MS m/z=171 [M+H]+. Calculated for C9H8F2O: 170.05.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296734B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-e79226b3c7cf420da0616f61fc115d28 |
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| Source note | uspto-grants-2016_03 |
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