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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843001Generated: November 4, 2026

Ethyl Acetate → Ethyl 2-(3-fluoro-4-(methylthio)phenyl)-2-oxoacetate

https://huagongshe.com/reaction/1843001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantEthoxalyl chlorideHCID 20884—
Reactant2-FluorothioanisoleHCID 2774762—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventChloroformHCID 6212—
SolventHexaneHCID 8058—
ProductEthyl 2-(3-fluoro-4-(methylthio)phenyl)-2-oxoacetateHCID 7081648364.6%

Reaction Steps

To a solution of AlCl3 (9.2 g, 0.06 mol, 2 eq) in chloroform (50 mL) cooled at 0° C., ethyl (chlorocarbonyl)formate (7.3 g, 0.05 mol, 1.6 eq) was added drop wise and the reaction mixture was stirred for 30-45 min at the same temperature. (2-fluorophenyl)(methyl)sulfane (5 g, crude) was added at 0° C. and the reaction mixture was stirred for 4 h at room temperature. Progress of the reaction was monitored by TLC (5% ethyl acetate in n-hexane, Rf˜0.5). On completion of the reaction, crushed ice was added and the mixture was stirred for some time. The organic layer was separated and the aqueous layer was extracted with DCM (2×50 mL). The combined extract was washed with NaHCO3 solution, dried over sodium sulfate and concentrated under reduced pressure to yield ethyl 2-(3-fluoro-4-(methylthio)phenyl)-2-oxoacetate as an yellow colored liquid (5.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946204B2
Source datasetuspto-grants-2015_02
ORD IDord-c9df38cf5c4142c6ada9906d18c3c7a8
Source noteuspto-grants-2015_02