HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylbenzylamine → 2-[Benzyl(methyl)amino]-1-(4-fluorophenyl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Chloro-4'-fluoroacetophenone | HCID 120248 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[Benzyl(methyl)amino]-1-(4-fluorophenyl)ethan-1-one | HCID 14459251 | 95.4% |
Reaction Steps
To a solution of benzyl-methyl-amine (28.9 g) and triethylamine (33.8 mL) in dimethylformamide (600 mL) was added in 5 portions 2-chloro-1-(4-fluorophenyl)-ethanone (40 g) on an ice bath. After stirring at room temperature for 2 hours, ethyl acetate was added, and the salt that precipitated was removed by filtration, and the filtrate was concentrated. A crude purification was carried out by silica gel column chromatography (hexane/ethyl acetate), and the title compound (56.9 g) was obtained as a colorless oily matter.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07217723B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-5ae767fe029b4d3ab468b43f9e5694cf |
| Source note | uspto-grants-2007_05 |