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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803966Generated: October 25, 2026

Tetrahydrofuran → (4-Bromophenyl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanone

https://huagongshe.com/reaction/1803966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromobenzoyl chlorideHCID 68515—
Reactant4-(4-Chlorobenzoyl)piperidine hydrochlorideHCID 2777114—
SolventEthyl AcetateHCID 8857—
Product(4-Bromophenyl)[4-(4-chlorobenzoyl)piperidin-1-yl]methanoneHCID 5848449799.3%

Reaction Steps

To tetrahydrofuran (120 mL) were added 4-bromobenzoyl chloride (25 g), (4-chlorophenyl)piperidin-4-ylmethanone hydrochloride (30 g) and 1N aqueous sodium hydroxide solution (250 mL), and the mixture was stirred at room temperature for 3 hr. Ethyl acetate was added for partitioning, the organic layer was washed with saturated brine, and the solvent was evaporated. The residue was recrystallized to give the title compound (46 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-c3cefcdddfc7477a9c5dc6cf4f6ff73d
Source noteuspto-grants-2013_01