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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717499Generated: October 27, 2026

Hexane → 2,5-Difluoro-4-[(methylsulfinyl)(methylthio)methyl]benzonitrile

https://huagongshe.com/reaction/1717499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantMethyl (methylsulfinyl)methyl sulfideHCID 99129—
Reactant2,4,5-TrifluorobenzonitrileHCID 593813—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2,5-Difluoro-4-[(methylsulfinyl)(methylthio)methyl]benzonitrileHCID 21904617—

Reaction Conditions

Temperature-78 °C

Reaction Steps

(Methylsulfinyl)(methylthio)methane (3.16 g, 0.0255 mol) was dissolved in 50 mL of dry THF under argon and then cooled to −78° C. Butyllithium in hexane (16 mL 1.6M, 0.0256 mol) was added dropwise with stirring. The mixture was stirred for 15 min. Meanwhile a solution of 2,4,5-trifluorobenzonitrile (2.0 g; 0.013 mol) in 50 mL of dry THF was cooled to −78° C. under argon and the former solution was added through a cannula to the latter solution over a period of 3-5 min. After 30 min, the cooling bath was removed and when the reaction had reached room temperature it was poured into 200 mL of water. The THF was evaporated and the remaining aqueous layer was extracted three times with diethyl ether. The combined ether phase washed with water, dried (Na2SO4) and evaporated. The crude product started to crystallise and could be used as such in the next step. Yield: 2.8 g (84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803954B2
Source datasetuspto-grants-2010_09
ORD IDord-0479cd1740d947729d5942d103d9c0a7
Source noteuspto-grants-2010_09