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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862489Generated: October 25, 2026

Hydrochloric Acid → Pyrazine, 2-phenyl-

https://huagongshe.com/reaction/862489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloropyrazineHCID 73277—
ReactantHCID 178418255HCID 178418255—
Catalyst[1,2-Bis(diphenylphosphino)ethane]dichloronickel(II)HCID 2734542—
SolventTetrahydrofuranHCID 8028—
ProductPyrazine, 2-phenyl-HCID 64287039%

Reaction Steps

Chloropyrazine (20.68 gram, 177 mmol) and [1,2-bis(diphenylphosphino)ethane]nickel(II) chloride (41.08 gram, 77.8 mmol) in dry THF (1.5 liter) were mixed and stirred for 80 minutes in a flask (cooled with a water bath) under nitrogen. A solution of phenylmagnesium bromide (3M in Et2O) (103 ml, 309 mmol) was added slowly through a dropping funnel into the cooled brick-red slurry at room temperature under nitrogen over 3.5 hours. After stirring at room temperature overnight, TLC showed that the reaction was complete. 3N HCl (100 ml) was added slowly through a dropping funnel under nitrogen and the mixture was stirred for one hour. The THF layer was separated from the aqueous layer. The aqueous layer was adjusted to pH 12 with 6N NaOH and extracted with EtOAc (100 ml, 3×). The organic fractions (THF and EtOAc) were combined and dried over MgSO4, filtered and concentrated to give a solid. The product was purified by flash chromatography on 300 g of flash grade silica gel in 2.5% EtOAc/CH2Cl2 to give 10.79 gram (69 mmol, 39%) of 2-phenylpyrazine, m.p. 69-70 C.; FAB mass [M+1]+ 157;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719156
Source datasetuspto-grants-1998_02
ORD IDord-d47e77ba037e456d9a65327f2f706bee
Source noteuspto-grants-1998_02