HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → N-(4-bromophenyl)-3-pyrrolidin-1-ylpropanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | n-(4-Bromophenyl)prop-2-enamide | HCID 263609 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(4-bromophenyl)-3-pyrrolidin-1-ylpropanamide | HCID 739898 | — |
Reaction Steps
N-(4-Bromo-phenyl)-acrylamide (0.3 g, 1.33 mmol) was dissolved in ethanol. Pyrrolidine (0.12 ml, 1.46 mmol) was added and the mixture was heated to reflux overnight. The solvent was removed under reduced pressure and the residue was dissolved in ethyl acetate. Aqueous ammonium chloride was added and the aqueous layer was extracted twice with ethyl acetate. The organics were combined, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to yield the desired product. Yield 0.24 g, 60%. LCMS method: 2, RT: 2.67 min; MI: 297-299 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09394301B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-33cc4cdc4a5b49d783460679f303907f |
| Source note | uspto-grants-2016_07 |