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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254414Generated: October 27, 2026

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

https://huagongshe.com/reaction/254414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
ReactantPyrrolidineHCID 31268—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium bicarbonate waterHCID 86585896—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromophenyl)-2-(1-pyrrolidinyl)ethanoneHCID 2138309549%

Reaction Steps

Diisopropylethylamine (6.2 mL, 36.0 mmol) and pyrrolidine (2.3 mL, 27.6 mmol) were added to a THF (90 mL) solution of 2-bromo-1-(4-bromophenyl)ethanone (5.0 g, 18.0 mmol), and stirred at room temperature for 2 hours. Saturated sodium bicarbonate water was added to the reaction liquid, extracted with chloroform, and dried with anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography (C-200, methanol:chloroform=1:99 to 3:97) to obtain the entitled compound (2.35 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875633B2
Source datasetuspto-grants-2011_01
ORD IDord-f6a4a4d4c30c4ac5a0a697930d9c6476
Source noteuspto-grants-2011_01