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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450075Generated: October 26, 2026

Iodoethane → 2-Propyl-3,4,5,6-tetrafluoropyridine

https://huagongshe.com/reaction/1450075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHexaneHCID 8058—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2,3,4,5-Tetrafluoro-6-methylpyridineHCID 15388342—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product2-Propyl-3,4,5,6-tetrafluoropyridineHCID 19691283—

Reaction Conditions

Temperature-60 °C

Reaction Steps

A 1.5M solution of LDA in hexane (100 mL, 150 mmol) is cooled to -60° C. in an isopropyl alcohol/dry ice bath. To the stirred LDA solution, under nitrogen, is added, dropwise over a 0.5 hours period, a solution of 22.617 g (137 mmol) of 3,4,5,6-tetrafluoro-2-picoline, the product of Step 1, in 80 mL of dry THF. The reaction mixture is stirred for 0.5 hours at -60° C. and then a solution of 10.95 mL (137 mmol) of ethyl iodide in 30 mL of dry THF is added, dropwise over a 20 minute period. After the reaction mixture is stirred at -60° C. for 0.5 hours, the cooling bath is allowed to slowly (1.5 hours) warm to -30° C. The reaction mixture is poured into cold brine and the aqueous mixture is extracted with methylene chloride. The organic extract is dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue is distilled to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599816
Source datasetuspto-grants-1997_02
ORD IDord-0a4023fa49f348e6bd9396afe9bf2614
Source noteuspto-grants-1997_02