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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698748Generated: October 31, 2026

Iodine → 2-t-Butoxy-3-iodopyrazine

https://huagongshe.com/reaction/1698748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantDiisopropylamineHCID 7912—
ReactantSodium SulfiteHCID 24437—
Reactant2-Tert-butoxypyrazineHCID 13256890—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-t-Butoxy-3-iodopyrazineHCID 872674186.2%

Reaction Steps

To a solution of 5.64 g of diisopropylamine in 100 ml of THF there was added 21.1 ml of n-butyllithium (2.55M, n-hexane solution) at −75° C. under a nitrogen atmosphere, and after stirring the mixture for 30 minutes, a solution of 6.78 g of 3-t-butoxypyrazine [CAS No. 70090-30-1] in 30 ml of THF was added dropwise. After stirring at the same temperature for 4 hours, a solution of 17.9 g of iodine in 100 ml of THF was added dropwise and the mixture was stirred overnight at room temperature. Next, 800 ml of saturated aqueous sodium sulfite and 800 ml of ethyl acetate were added, and the organic layer was washed with 300 ml of saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane-ethyl acetate) to give 2-t-butoxy-3-iodopyrazine (0.77 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163787B2
Source datasetuspto-grants-2012_04
ORD IDord-9f6a50605b144f2c9572db7ca3933e6e
Source noteuspto-grants-2012_04