HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246677Generated: October 27, 2026
Hexane → 2,5-Difluoro-4-[(methylsulfinyl)(methylthio)methyl]benzonitrile
https://huagongshe.com/reaction/1246677
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Methyl (methylsulfinyl)methyl sulfide | HCID 99129 | — |
| Reactant | 2,4,5-Trifluorobenzonitrile | HCID 593813 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,5-Difluoro-4-[(methylsulfinyl)(methylthio)methyl]benzonitrile | HCID 21904617 | — |
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 was 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129233B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-fa1d23c1ebdd48b8b8c9ea7a0e9959a4 |
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| Source note | uspto-grants-2006_10 |
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