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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528289Generated: November 4, 2026

Benzaldehyde → (1S,2S)-N-benzylcyclohexane-1,2-diamine

https://huagongshe.com/reaction/1528289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantMethanolHCID 887—
Reactant1,2-Diaminocyclohexane, (+)-HCID 479307—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Product(1S,2S)-N-benzylcyclohexane-1,2-diamineHCID 7061051648%

Reaction Steps

Benzaldehyde (3.05 mL, 30.0 mmol) was added to a methanol (300 mL) solution of (1S,2S)-cyclohexane-1,2-diamine (3.43 g, 30.0 mmol) with stirring at room temperature, and the mixture was stirred overnight at the same temperature. The reaction mixture was cooled to 0° C. Sodium borohydride (2.27 g, 60.0 mmol) was added thereto, and the mixture was stirred at 0° C. for 2 hours. To the reaction mixture, water (30 mL) was added, and the product was extracted twice with methylene chloride (50 mL). The organic layers were combined and dried over magnesium sulfate, and the solvent was then distilled off under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate/hexane) to obtain (1S,2S)-N-benzylcyclohexane-1,2-diamine (cas no. 207450-11-1) (2.95 g, yield: 48%) in a pale yellow oil form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090572B2
Source datasetuspto-grants-2015_07
ORD IDord-4cf198e4c3ba453d81b511f70db8e6c6
Source noteuspto-grants-2015_07