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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458125Generated: October 25, 2026

Dimethyl Sulfide → 4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-one

https://huagongshe.com/reaction/458125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantMesityl oxideHCID 8858—
Reactant2-Bromo-4-fluoroanisoleHCID 136292—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-oneHCID 2228492285%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 2-bromo-4-fluoro anisole (3.24 mL, 25 mmol) in anhydrous THF (40 mL) cooled to −78° C. and maintained under argon was added n-butyl lithium (17.2 mL of 1.6 M solution in hexanes, 27.5 mmol). After stirring at −78° C. for 45 minutes, the reaction mixture was treated with a solution of cuprous iodide in dimethyl sulfide (4.76 g in 15 mL, 25 mmol) and stirred for 15 minutes at −78° C. Then chlorotrimethylsilane (6.4 mL, 50 mmol) was added, followed by a solution of mesityl oxide (2.9 mL, 25 mmol) in anhydrous THF (5 mL). The reaction was stirred at −78° C. to −60° C. for 4 hours and then quenched with a saturated solution of ammonium chloride and extracted with three 50 mL portions of methylene chloride. The combined extracts were washed with three 25 mL portions of water, dried over anhydrous sodium sulfate, and concentrated in vacuo to give 4-(5-fluoro-2-methoxyphenyl)-4-methylpentan-2-one as a light brown liquid (85% yield) which was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189758B2
Source datasetuspto-grants-2007_03
ORD IDord-c8ea7327285d4c5887ed3c45b93c981d
Source noteuspto-grants-2007_03