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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179304Generated: November 1, 2026

Dimethyl Disulfide → 4-Fluoro-2-methylsulfanyl-benzoic acid

https://huagongshe.com/reaction/1179304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl DisulfideHCID 12232—
Reactant2-Bromo-4-fluorobenzoic acidHCID 1268169—
ReactantHCID 178418332HCID 178418332—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Fluoro-2-methylsulfanyl-benzoic acidHCID 16228032—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 2-bromo-4-fluorobenzoic acid (15 g, 68.5 mmol, Marshallton Research Laboratories) in THF (150 mL) under argon at 0° C. was treated with chloro(methyl)magnesium (5.64 g, 75.34 mmol, 2.94 M in THF) over 5 minutes. The temperature during addition was maintained below 10° C. The resulting solution was cooled to −78° C. and n-butyllithium (9.65 g, 150.7 mmol, 2.5M in hexanes) was added over 10 minutes. The reaction was kept below −65° C. during the addition. The reaction was stirred at −78° C. for 50 minutes. A solution of (methyldithio)methane (38.71 g, 410.9 mmol) in THF (20 mL), precooled to −78° C., was added by cannula. The reaction was stirred for 10 minutes, warmed to zero ° C. and stirred at zero ° C. for 2 hours until a solid began to precipitate. The reaction was allowed to warm to 25° C. and stirred overnight. The reaction was poured into 1N HCl and extracted with EtOAc. The water layer was extracted with EtOAc twice more, the organic layers were combined, dried over Na2SO4, filtered and evaporated. The crude solid was suspended in 5% EtOAc/Hexanes and stirred for an hour, then filtered and dried to give the product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279487B2
Source datasetuspto-grants-2007_10
ORD IDord-0d78e96069fc4fd6b3ce61963c562c9d
Source noteuspto-grants-2007_10