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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178501210HCID 178501210—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-Benzylamino-cyclohexanecarboxylic acid methyl esterHCID 2162799647%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691756B2
Source datasetuspto-grants-2014_04
ORD IDord-8ba29f82b691470d82f549acfb926b9e
Source noteuspto-grants-2014_04