HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethylamine → 2-(3,4-dimethoxyphenyl)-N-(2-phenylethyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | (3,4-Dimethoxyphenyl)acetic acid | HCID 7139 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3,4-dimethoxyphenyl)-N-(2-phenylethyl)acetamide | HCID 297246 | 80.3% |
Reaction Steps
A solution of 3,4-dimethoxyphenylacetic acid (17.1 g, 0.090 mol) and carbonyldiimidazole (14.6 g, 0.090 mol) in THF (200 ml) was stirred for 2.5 h in a flask fitted with a drying tube. To this solution was added 2-phenylethylamine (10.9 g, 0.090 mol) in THF (50 ml). After 1 h the THF was evaporated and the residue was treated with water (200 ml) and filtered. The crude amide was washed with water and recrystallized from mixture of 200 ml of methanol and 100 ml of water with a charcoal treatment to afford 21.6 g (80.3%) of the title compound mp 123-124°. A second crop (2.1 g, 7.8%) was obtained after concentrating the mother liquors.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04956371 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-5e52046eb7ea4098a811b1fe15843faa |
| Source note | uspto-grants-1990_09 |