HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylephedrine → Metamfepramone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylephedrine | HCID 4374 | — |
| Reactant | 2-Iodobenzoic acid | HCID 6941 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Metamfepramone | HCID 71872 | 93% |
Reaction Steps
N-Methylephedrine (500 mg, 2.79 mmol) was added to a solution of o-iodobenzoic acid I (7.8 g; 27.9 mmol) in DMSO (55 ml). After 48 hours the solution was diluted with NaHCO3 (2.5%, 30 ml) and extracted with ethyl acetate (3×10 ml). The combined organic layers were washed with water (2×5 ml), dried over sodium sulfate and evaporated to dryness under vacuum. The residue was purified by distillation to give 460 mg (92%) of 2-dimethylamino-1-phenyl-propan-1-one (boiling at 113°-117° C./12 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05510538 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-23aa75153c324d239afd01507e1b0edb |
| Source note | uspto-grants-1996_04 |