HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl formate → Methyl 3-hydroxy-2-(2-benzoylpyrrol-1-yl)acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 2-(2-benzoylpyrrol-1-yl)acetate | HCID 6618880 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-hydroxy-2-(2-benzoylpyrrol-1-yl)acrylate | HCID 67826680 | 86.2% |
Reaction Steps
Sodium hydride (1.44 g, 55% in oil, 0.033 mol) was washed with petrol 60°-80° and suspended in DMF (15 ml). To this the methyl (2-benzoylpyrrol-1-yl)acetate (4.0 g, 0.0165 mol) in DMF (15 ml) and methyl formate (20.3 ml, 0.33 mol) was added dropwise at room temperature. After 4 hours it was poured into 200 ml of 10% potassium carbonate, washed with diethyl ether (2×100 mls), then the aqueous was neutralised with concentrated hydrochloric acid and extracted with diethyl ether (2×100 ml). These extracts were washed with brine, dried and evaporated to give methyl 3-hydroxy-2-(2-benzoylpyrrol-1-yl)acrylate (3.86 g, 86%) as a white crystalline solid melting at 112°-113° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05091407 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-4a39feb2340945f98ea1c61de19fba71 |
| Source note | uspto-grants-1992_02 |