HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethylamine → N1-phenethyl-4-bromo-2-methoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromo-2-methoxybenzoyl chloride | HCID 22346782 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N1-phenethyl-4-bromo-2-methoxybenzamide | HCID 22346935 | 90.1% |
Reaction Steps
Phenethylamine (0.79 mL, 6.31 mmol) was added slowly to a mixture of 4-Bromo-2-methoxy-1-benzenecarbonyl chloride (1.5 g, 6.01 mmol) and triethylamine (1.3 mL, 9.02 mmol) in dichloromethane (60 mL). After 2 hours, solvent was removed under reduced pressure. Ethyl acetate was added and the mixture was filtered. The filtrate was concentrated under reduced pressure and the residue was purified by flash column chromatography using dichloromethane/ethyl acetate (97:3) as mobile to give N1-phenethyl-4-bromo-2-methoxybenzamide (1.81 g, 90%). 1H NMR (DMSO-d6) δ 2.83 (m, 2H), 3.50 (m, 2H), 3.84 (s, 3H), 7.31 (m, 7H), 7.65 (d, J=8.28 Hz, 1H), 8.15 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06660744B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-d07c2f44ff5d4c94920b1f54caec2816 |
| Source note | uspto-grants-2003_12 |