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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472816Generated: October 30, 2026

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

https://huagongshe.com/reaction/1472816

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 numberUS09012633B2
Source datasetuspto-grants-2015_04
ORD IDord-4cdc35ea5fe5468ab2d352aa1b6fe650
Source noteuspto-grants-2015_04