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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 444715Erstellt: 24. Oktober 2026

Benzaldehyde → 4-Benzylamino-cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/de/reaction/444715

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
EduktSodium borohydrideHCID 4311764—
EduktHCID 178501210HCID 178501210—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt4-Benzylamino-cyclohexanecarboxylic acid methyl esterHCID 2162799647%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476224B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-b38515c7b60840769501d950406c8163
Quellennotizuspto-grants-2013_07