HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-Bromophenyl)-2-chloroacetamide → N-(4-bromophenyl)-2-(pyrrolidin-1-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-Bromophenyl)-2-chloroacetamide | HCID 17374 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(4-bromophenyl)-2-(pyrrolidin-1-yl)acetamide | HCID 1091709 | — |
Reaction Steps
N-(4-Bromo-phenyl)-2-chloro-acetamide (0.3 g, 1.21 mmol) was dissolved in anhydrous toluene (10 ml). Pyrrolidine (0.3 ml, 3.63 mmol) was added dropwise to the mixture, which was then heated to reflux and stirred overnight. The toluene was removed under reduced pressure and the residue was dissolved in ethyl acetate. Saturated ammonium chloride was added and the aqueous layer was extracted twice with ethyl acetate. The organics were combined, washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. Yield 0.22 g, 65%. LCMS method: 2, RT: 2.62 min; MI: 283-285 [M+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09012633B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-4cdc35ea5fe5468ab2d352aa1b6fe650 |
| Source note | uspto-grants-2015_04 |