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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354328Generated: October 27, 2026

4-Bromophenacyl bromide → 1-(4-Bromophenyl)-2-(1-pyrrolidinyl)ethanone

https://huagongshe.com/reaction/2354328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
ReactantPyrrolidineHCID 31268—
SolventDiethyl EtherHCID 3283—
Product1-(4-Bromophenyl)-2-(1-pyrrolidinyl)ethanoneHCID 2138309596%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-bromo-1-(4-bromophenyl)ethanone (5.0 g, 18 mmol) was dissolved in 10 mL diethyl ether and added dropwise over 15 min to a solution of pyrrolidine (3.0 mL, 36 mmol) in 20 mL diethyl ether cooled to 0° C. in an ice bath. The resulting solution was allowed to warm to room temperature and maintained for 1 h. The solvent was removed under reduced pressure. The residue was dissolved in 100 mL of EtOAc and washed with sodium bicarbonate (100 mL) and then brine (100 mL). The organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure to give 4.6 g (96%) of the title compound as a yellow/orange solid. MS (ES) m/e 268/270 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07749998B2
Source datasetuspto-grants-2010_07
ORD IDord-29b3e73253d842a1af650f83bebb1ca4
Source noteuspto-grants-2010_07