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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835233Generated: October 27, 2026

Allyl bromide → Pyrazine, 3-butenyl-

https://huagongshe.com/reaction/1835233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant2-MethylpyrazineHCID 7976—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamineHCID 45051747—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductPyrazine, 3-butenyl-HCID 22477625—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of lithium diisopropylamine [prepared from a solution of butyl lithium in hexanes (100 mL, 2.5M) and diispropylamine (25.3 g) at −35° C.] was treated with a solution of 2-methylpyrazine (23.5 g) in dry tetrahydrofuran (300 mL) at −20° C. The mixture was stirred at −20° C. for 1 hour then cooled to −78° C. and treated with a solution of allyl bromide (30.8 g) in dry tetrahydrofuran (300 mL). This mixture was warned to room temperature and stirred at this temperature for 2 hours then left overnight and then treated with saturated ammonium chloride solution (50 mL) followed by water (200 mL). The mixture was then extracted twice with ether (200 mL). The combined extracts were dried over magnesium sulfate then evaporated. The residue was distilled to give the title compound (22 g) as a colorless oil, b.p. 70° C./1 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770643B2
Source datasetuspto-grants-2004_08
ORD IDord-63544658ec604169b91df5fd092f4a57
Source noteuspto-grants-2004_08