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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2181035Erstellt: 25. Oktober 2026

3-Chloro-4-methylaniline → 3-chloro-N-cyclohexylmethyl-4-methylaniline

https://huagongshe.com/reaction/2181035

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Chloro-4-methylanilineHCID 7255—
EduktCyclohexanecarboxaldehydeHCID 16275—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
Produkt3-chloro-N-cyclohexylmethyl-4-methylanilineHCID 2248516285,3%

Reaktionsschritte

To a solution of 3-chloro-4-methylaniline (7.08 g) in methanol (35 ml) were added cyclohexanecarbaldehyde (5.33 g) and sodium cyanoborohydride (3.78 g) under ice-cooling and the mixture was stirred at room temperature. After one hour, the reaction mixture was concentrated and water and saturated brine were added. The mixture was extracted 3 times with ethyl acetate. The organic layers were combined, washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified by column chromatography (silica gel, hexane/ethyl acetate=15/1) to give 3-chloro-N-cyclohexylmethyl-4-methylaniline as a pale-yellow oil (9.64 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06890934B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-d70075e51e554e93bf0665831b220bc7
Quellennotizuspto-grants-2005_05