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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472818Generated: October 30, 2026

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

https://huagongshe.com/reaction/1472818

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 numberUS09012633B2
Source datasetuspto-grants-2015_04
ORD IDord-f12cab27300c4515b1e067ffd0cd98aa
Source noteuspto-grants-2015_04