Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054366Generated: October 29, 2026

Pyrrolidine → N-(4-bromophenyl)-3-pyrrolidin-1-ylpropanamide

https://huagongshe.com/reaction/1054366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactantn-(4-Bromophenyl)prop-2-enamideHCID 263609—
SolventEthanolHCID 702—
ProductN-(4-bromophenyl)-3-pyrrolidin-1-ylpropanamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394301B2
Source datasetuspto-grants-2016_07
ORD IDord-33cc4cdc4a5b49d783460679f303907f
Source noteuspto-grants-2016_07