HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Carbonate → Ethyl 2-(pyrimidin-4-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Carbonate | HCID 7766 | — |
| Reactant | 4-Methylpyrimidine | HCID 18922 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Product | Ethyl 2-(pyrimidin-4-yl)acetate | HCID 20295406 | 78.1% |
Reaction Steps
To a flask containing LiHMDS (32 mL, 31.89 mmol, 1.0 M in THF) at −70° C., was slowly added 4-methylpyrimidine (1.0 g, 10.63 mmol). After 5 min of stirring at −70° C. diethylcarbonate (1.93 mL, 15.95 mmol) was added, the reaction was slowly warmed to room temperature and stirred for 4 days. The reaction mixture was quenched by addition of 1 N HCl, neutralized with saturated aqueous NaHCO3 and extracted with EtOAc (3×). The combined organics were dried over Na2SO4, filtered, concentrated under reduced pressure and purified by flash chromatography on silica gel (0-100% EtOAc in hexanes) to give the title compound as a yellow oil (1.38 g, 78%). MS 167 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09138013B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-3f4ac38ae6694318aabe41a140737262 |
| Source note | uspto-grants-2015_09 |