HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 14326177, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 19785053 | HCID 19785053 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14326177 | HCID 14326177 | 79% |
Reaction Steps
A solution of methyl pyrrol-3-yloxoacetate (3.3 g. 22 mol) in THF (70 ml) was added at room temperature to a stirred suspension of potassium tert-butoxide (2.7 g, 24 mmol) and 18-crown-6 (0.1 g, 0.39 mmol) in ether (250 ml). The reaction mixture was stirred for 30 minutes then iodomethane (1.6 ml, 26 mmol) in ether (50 ml) was added dropwise. The reaction mixture was stirred for 16 hours then filtered through hyflo supercell and washed with brine, dried and concentrated to give methyl N-methyl-pyrrol-3-yloxoacetate (2.84 g, 79% yield) as a clear oil, IR (thin film) 1725, 1645 cm-1, 1H nmr: delta 3.64 (3H, s), 3.85 (3H, s), 6.5 (1H, m) 6.7 (1H, m), 7.6 (1H, m) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05053073 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-6d7664cefc3a46218629ac3519995381 |
| Source note | uspto-grants-1991_10 |