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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648507Generated: October 27, 2026

Triethylamine → 4-(4-Fluorobenzoyl)-1-(4-nitrobenzoyl)piperidine

https://huagongshe.com/reaction/648507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
Reactantp-Fluorophenyl 4-piperidyl ketone hydrochlorideHCID 3084438—
SolventDichloromethaneHCID 6344—
Product4-(4-Fluorobenzoyl)-1-(4-nitrobenzoyl)piperidineHCID 1360396585.5%

Reaction Steps

4-Nitrobenzoyl chloride (3.08 g) was added slowly to a stirred mixture of 4-(4-fluorobenzoyl)piperidine hydrochloride (4.0 g) and triethylamine (4.98 g) in methylene chloride (110 ml) at room temperature. The resulting mixture was stirred at this temperature for 1 hour, washed with 1N hydrochloric acid, saturated sodium bicarbonate solution, and brine, dried over magnesiun sulfate and concentrated in vacuo. The residue was recrystallized from a mixture of acetone and methanol to give 4-(4-fluorobenzoyl)-1-(4-nitrobenzoyl)piperidine (5.0 g) as colourless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735952
Source datasetuspto-grants-1988_04
ORD IDord-62f909a151c64ea7bb61e29664fb3cbd
Source noteuspto-grants-1988_04