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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898839Generated: October 29, 2026

Diethyl Malonate → Diethyl 2-[1-(4-fluorophenyl)-1-methyl-2-methylsulfanyl-ethyl]malonate

https://huagongshe.com/reaction/898839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantEthanol sodium ethoxideHCID 23706232—
Reactant1-(2-Chloro-1-methyl-1-methylsulfanyl-ethyl)-4-fluorobenzeneHCID 59692380—
Reactant1-(1-Chloro-1-methyl-2-methylsulfanyl-ethyl)-4-fluorobenzeneHCID 59692580—
SolventEthanolHCID 702—
ProductDiethyl 2-[1-(4-fluorophenyl)-1-methyl-2-methylsulfanyl-ethyl]malonateHCID 5969240284%

Reaction Steps

To a solution of diethyl malonate (12 mL, 81 mmol) in ethanol (40 mL) was added dropwise 21% sodium ethoxide ethanol solution (29 mL, 77 mmol) under nitrogen atmosphere under ice-cooling. The mixture was warmed to room temperature, stirred for 1 hour, and cooled again with ice. The crude product (73 mmol) of 1-(1-chloro-1-methyl-2-methylsulfanyl-ethyl)-4-fluorobenzene or 1-(2-chloro-1-methyl-1-methylsulfanyl-ethyl)-4-fluorobenzene obtained in Example 1-3 was added dropwise to the mixture while maintaining a temperature below 4° C. The obtained solution was stirred for 1 hour at room temperature and concentrated under reduced pressure. The residue was neutralized by adding a 2N aqueous hydrochloric acid solution and the aqueous layer was extracted with ethyl acetate (50 mL). The organic layer was dried over magnesium sulfate, filtrated and the solvent was evaporated. Then the obtained residue was purified by silica gel chromatography (hexane:ethyl acetate=20:1 to 5:1) to give the title compound (24 g, yield 84%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351825B2
Source datasetuspto-grants-2008_04
ORD IDord-f79963e9fb9d489c87652dae8595c891
Source noteuspto-grants-2008_04