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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054364Generated: November 1, 2026

N-(4-Bromophenyl)-2-chloroacetamide → N-(4-bromophenyl)-2-(pyrrolidin-1-yl)acetamide

https://huagongshe.com/reaction/1054364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Bromophenyl)-2-chloroacetamideHCID 17374—
ReactantPyrrolidineHCID 31268—
SolventTolueneHCID 1140—
ProductN-(4-bromophenyl)-2-(pyrrolidin-1-yl)acetamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394301B2
Source datasetuspto-grants-2016_07
ORD IDord-d7d0aa4d08d54da38e7745113f6d17b2
Source noteuspto-grants-2016_07