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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,2-Diaminocyclohexane, (+)- | HCID 479307 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Product | (1S,2S)-N-benzylcyclohexane-1,2-diamine | HCID 70610516 | 48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090572B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-4cf198e4c3ba453d81b511f70db8e6c6 |
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| Source note | uspto-grants-2015_07 |
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