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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623902Generated: October 29, 2026

Ammonium Chloride → 5-Chloropyrazine-2-carbaldehyde

https://huagongshe.com/reaction/623902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 5-chloropyrazine-2-carboxylateHCID 406081—
ReactantHCID 21273587HCID 21273587—
SolventTetrahydrofuranHCID 8028—
Product5-Chloropyrazine-2-carbaldehydeHCID 2169806735.6%

Reaction Steps

In tetrahydrofuran (66 mL) was dissolved methyl 5-chloropyrazine-2-carboxylate (3.3 g), and 1M diisobutylaluminum hydride/hexane solution (38.3 mL) was added dropwise to the solution under nitrogen atmosphere at −70° C. or lower over 10 minutes, and the resulting mixture was further stirred for 10 minutes. At −60° C. or lower, 1M diisobutylaluminum hydride/hexane solution (31.3 mL) was added dropwise to the mixture over 20 minutes, and the mixture was further stirred at −70° C. or lower for 1 hour. The reaction mixture was poured into a saturated aqueous ammonium chloride solution, and after stirring at room temperature, filtered with Celite. The filtrate was extracted with ethyl acetate, washed with a saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0 to 80:20) to obtain 5-chloropyrazine-2-carbaldehyde (970 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302996B2
Source datasetuspto-grants-2016_04
ORD IDord-487c38dd4bec43b183ca8b5e03da5e79
Source noteuspto-grants-2016_04