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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387051Generated: November 4, 2026

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

https://huagongshe.com/reaction/1387051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Bromophenyl)-2-chloroacetamideHCID 17374—
ReactantPyrrolidineHCID 31268—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-bromophenyl)-2-(pyrrolidin-1-yl)acetamideHCID 1091709—

Reaction Steps

A solution of 5.0 g (0.02 mol) of N-(4-bromophenyl)-α-chloroacetamide (Part A) and 5.05 mL (0.06 mol) of pyrrolidine in 100 mL of THF was stirred overnight at ambient temperature. The mixture was concentrated in vacuo and the residue was partitioned between H2O and EtOAc. The organic layer was separated, washed with H2O, dried over Na2SO4, filtered, and evaporated in vacuo to afford 5.74 g of analytically pure title compound as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-846bec2310514558b4c8c7ac7758e998
Source noteuspto-grants-2001_07