HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → Methyl 4-benzyl-3-oxo-3,4-dihydropyrazine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | Methyl 3-hydroxypyrazine-2-carboxylate | HCID 1514283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-benzyl-3-oxo-3,4-dihydropyrazine-2-carboxylate | HCID 67348566 | 64.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003662B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-cd58a96de237414f9ca7a8fa7094678c |
| Source note | uspto-grants-2011_08 |