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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021393Generated: October 31, 2026

4-(4-Chlorophenyl)butanamide → 4-(4-Chlorophenyl)butan-1-amine

https://huagongshe.com/reaction/1021393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorophenyl)butanamideHCID 11074357—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Chlorophenyl)butan-1-amineHCID 1077382261%

Reaction Steps

To a stirred suspension of lithium aluminum hydride (1.84 g, 48.6 mmol) in diethyl ether (50 mL) at ambient temperature was added a solution of 4-(4-chlorophenyl)butanamide in tetrahydrofuran (25 mL), dropwise over 8 minutes. Stirring was continued at ambient temperature for a further 4 hours. The reaction mixture was carefully quenched by sequential slow addition of water (2 mL), 10M sodium hydroxide (0.75 mL), and water (7 mL). After stirring the mixture for 20 minutes, it was extracted with diethyl ether (50 mL). The organic layer was dried over sodium sulfate and concentrated to afford 4-(4-chlorophenyl)butan-1-amine as a light yellow oil (1.36 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716498B2
Source datasetuspto-grants-2014_05
ORD IDord-b16e619b081e43e1b797b1a2abaa452b
Source noteuspto-grants-2014_05