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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071632Generated: November 2, 2026

Sodium Iodide → 4-Cyano-5-methyl-4-(3-cyano-2-thienyl)hexyl iodide

https://huagongshe.com/reaction/1071632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Cyano-5-methyl-4-(3-cyano-2-thienyl)hexanolHCID 22393634—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
Product4-Cyano-5-methyl-4-(3-cyano-2-thienyl)hexyl iodideHCID 2239382695.1%

Reaction Steps

244 mg (0.98 mmol) of 4-cyano-5-methyl-4-(3-cyano-2-thienyl)hexanol was dissolved in 10 ml of acetonitrile and 0.16 ml (1.18 mmol) of triethylamine, and 83.6 μl (108 mmol) of mesyl chloride was added thereto. After about 5 minutes, 1.47 g (9.80 mmol) of sodium iodide was added. After completion of the reaction, brine and ethyl acetate were added, and the ethyl acetate layer was washed with an aqueous sodium thiosulfate aqueous solution and brine, dried over anhydrous magnesium sulfate and evaporated, to give a crude product. The crude product was subjected to silica gel (eluted at ethyl acetate:hexane=1:10), to give 334 mg (0.93 mmol, 95.1%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906072B1
Source datasetuspto-grants-2005_06
ORD IDord-b6ea499660b24c42b2a23b466c9f051e
Source noteuspto-grants-2005_06