HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → Diethyl [(2-methyl-4-phenyl-1,3-oxazol-5-yl)methyl]propanedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-(Bromomethyl)-2-methyl-4-phenyl-1,3-oxazole | HCID 13293291 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl [(2-methyl-4-phenyl-1,3-oxazol-5-yl)methyl]propanedioate | HCID 13646801 | 66.2% |
Reaction Steps
60% Sodium hydride in oil (1.48 g) was added portionwise to a solution of diethyl malonate (11.7 g) in N,N-dimethylformamide (50 ml) and the mixture was stirred for 10 minutes. A solution of 5-bromomethyl-2-methyl-4-phenyloxazole (9.2 g) in N,N-dimethylformamide (20 ml) was added dropwise under ice-cooling. The mixture was stirred under ice-cooling for 30 minutes, diluted with water, and extracted with ethyl ether. The ethyl ether layer was washed with water and dried over anhydrous sodium sulfate. The solvent was then distilled off and the residue was purified by silica gel chromatography [silica gel: 120 g; eluent: hexane-ethyl ether (3:2)] to give an oil (8.0 g) of diethyl 2-(2-methyl-4-phenyl-5-oxazolylmethyl)malonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04596816 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-c61749d4317c40b98b21f53403bb6a5b |
| Source note | uspto-grants-1986_06 |