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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930415Generated: November 1, 2026

Ethyl fluoroacetate → HCID 86732254, compound

https://huagongshe.com/reaction/930415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl fluoroacetateHCID 9988—
Reactant3-Bromo-2-fluorotolueneHCID 108855—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86732254HCID 8673225480%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-e79226b3c7cf420da0616f61fc115d28
Source noteuspto-grants-2016_03