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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025398Generated: November 2, 2026

Benzaldehyde → 3-(azepan-1-yl)-N-benzyl-N-methylpropan-1-amine

https://huagongshe.com/reaction/1025398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
Reactant3-(Azepan-1-yl)propan-1-amineHCID 2764395—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
Product3-(azepan-1-yl)-N-benzyl-N-methylpropan-1-amineHCID 58540516—

Reaction Steps

To a mixture of 3-(Azepan-1-yl)propan-1-amine (0.10 g, 0.64 mmole) in methylene chloride (5 mL) were added benzaldehyde (0.64 mmole) and NaBH(OAc)3 (0.63 g, 3.0 mmol). The reaction solution was stirred at room temperature for 3 h. Then, paraformaldehyde (200 mg) was added to the reaction mixture and stirring was continued for 6 h. 2N aqueous NaOH (2 mL) was added to quench the reaction, followed by addition of methylene chloride (30 mL). The organic layer was separated, dried over anhydrous Na2SO4, and filtered. The filtrate was evaporated to supply 3-(azepan-1-yl)-N-benzyl-N-methylpropan-1-amine (151 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729081B2
Source datasetuspto-grants-2014_05
ORD IDord-f21b74ff1a3e4dc2a06628c956941480
Source noteuspto-grants-2014_05