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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676357Generated: October 27, 2026

Benzyl Chloride → Methyl 4-benzyl-3-oxo-3,4-dihydropyrazine-2-carboxylate

https://huagongshe.com/reaction/1676357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantLithium hydrideHCID 62714—
ReactantMethyl 3-hydroxypyrazine-2-carboxylateHCID 1514283—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-benzyl-3-oxo-3,4-dihydropyrazine-2-carboxylateHCID 6734856664.2%

Reaction Steps

LiH (7.8 mg, 0.980 mmol) was added to the solution of methyl 3-oxo-3,4-dihydropyrazine-2-carboxylate (100 mg, 0.65 mmol) in DMF (3 mL) at 0° C. After 30 minutes stirring, (chloromethyl)benzene (0.15 mL, 1.30 mmol) was added to the reaction mixture at 0° C., and then the reaction was warmed to room temperature. After 4 hours stirring, the reaction mixture was quenched with ice water, extracted with EtOAc, washed with brine, dried over MgSO4, and concentrated to give the crude material that was purified by silica gel flash column chromatography (2% MeOH in CH2Cl2) to afford 0.102 g (64%) of the desired product. 1H-NMR (400 MHz, CDCl3) δ 7.38 (m, 6H), 7.29 (d, 1H), 5.14 (s, 2H), 3.98 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003662B2
Source datasetuspto-grants-2011_08
ORD IDord-cd58a96de237414f9ca7a8fa7094678c
Source noteuspto-grants-2011_08