HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361583Generated: October 26, 2026
Benzaldehyde → 4-Benzylamino-cyclohexanecarboxylic acid methyl ester
https://huagongshe.com/reaction/2361583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178501210 | HCID 178501210 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Benzylamino-cyclohexanecarboxylic acid methyl ester | HCID 21627996 | 47% |
Reaction Steps
To a solution of trans-4-amino-cyclohexylcarboxylic acid methyl ester hydrochloride (4.5 g, 23.24 mmol) in MeOH (30 mL) is added TEA (1.3 mL, 9.339 mmol), MgSO4 (4.2 g, 34.88 mmol), and benzaldehyde (2.5 mL, 24.74 mmol). The mixture stirs 1 h. The mixture is then cooled to 0° C. and NaBH4 (5.0 g, 132.2 mmol) is added portionwise over 0.5 h. The mixture stirs 1 h at ambient temperature. Then H2O (200 mL) is added and the mixture is extracted with EtOAc (2×500 mL), dried and concentrated. The resulting solid is purified by flash chromatography (gradient elution: 0-100% EtOAc/Hep) which affords 2.7 g of 4-benzylamino-cyclohexanecarboxylic acid methyl ester. LC/MS: [M+H]+ 248, Rt=0.82 min (method 11).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691756B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-8ba29f82b691470d82f549acfb926b9e |
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| Source note | uspto-grants-2014_04 |
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