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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890051Generated: November 1, 2026

Water → 6-(tert-Butoxy)pyrazine-2-carbaldehyde

https://huagongshe.com/reaction/890051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium SulfiteHCID 24437—
Reactant2-Tert-butoxy-6-vinylpyrazineHCID 22248276—
Solventtert-ButanolHCID 6386—
Product6-(tert-Butoxy)pyrazine-2-carbaldehydeHCID 2224827396%

Reaction Steps

After adding 7.20 g of AD-mix-5 to 60 ml of 50% aqueous tert-butanol, a solution of 1.00 g of 2-tert-butoxy-6-vinylpyrazine in tert-butanol (5 ml) was added and the mixture was stirred overnight at room temperature. Next, 8.40 g of sodium sulfite was added to the reaction solution, the mixture was stirred at room temperature for 1 hour, and then water was added and extraction was performed with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was dissolved in 40 ml of methanol, an aqueous solution of 2.35 g of sodium periodate (20 ml) was added while stirring on ice, and stirring was continued at room temperature for 40 minutes. Water was added to the reaction solution, and extraction was performed with ethyl acetate. The extract was washed with water and saturated brine and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (954 mg, 96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995144B2
Source datasetuspto-grants-2006_02
ORD IDord-1062e21b55a34952a9e4008e18c2dc8b
Source noteuspto-grants-2006_02