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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510627Generated: November 1, 2026

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

https://huagongshe.com/reaction/510627

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 numberUS09096567B2
Source datasetuspto-grants-2015_08
ORD IDord-c58cc3f3fba747f983ac889d096599ce
Source noteuspto-grants-2015_08