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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440988Generated: October 31, 2026

Sodium Iodide → 5-(3-Trifluoromethylphenyl)hexanenitrile

https://huagongshe.com/reaction/440988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetonitrileHCID 6342—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantHCID 19955494HCID 19955494—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
Product5-(3-Trifluoromethylphenyl)hexanenitrileHCID 1995551546.3%

Reaction Steps

Under a nitrogen atmosphere, a solution of 4.4 grams (0.017 mole) of 5-hydroxy-5-(3-trifluoromethylphenyl)hexanenitrile, 13 mL (0.102 mole) of chlorotrimethylsilane, 15.4 grams (0.102 mole) of sodium iodide, and 8.0 mL (0.153 mole) of acetonitrile in 30 mL of hexane was stirred for about 30 minutes. After this time, gas chromatographic analysis of the reaction mixture indicated that the reaction was complete. The reaction mixture was then stirred with 100 mL of water, and then it was extracted with 100 mL of diethyl ether. The combined extracts were dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was subjected to column chromatography on silica gel. Elution was accomplished using methylene chloride. The methylene chloride eluate was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 1.9 grams of 5-(3-trifluoromethylphenyl)hexanenitrile. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521192
Source datasetuspto-grants-1996_05
ORD IDord-615c506ae4684bf5a8edd96d9640b33a
Source noteuspto-grants-1996_05