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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971551Generated: November 4, 2026

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

https://huagongshe.com/reaction/1971551

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 numberUS08431596B2
Source datasetuspto-grants-2013_04
ORD IDord-2c80ca0214f74018ab7965bd44d4cd1b
Source noteuspto-grants-2013_04