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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181035Generated: October 25, 2026

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

https://huagongshe.com/reaction/2181035

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-methylanilineHCID 7255—
ReactantCyclohexanecarboxaldehydeHCID 16275—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Product3-chloro-N-cyclohexylmethyl-4-methylanilineHCID 2248516285.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06890934B2
Source datasetuspto-grants-2005_05
ORD IDord-d70075e51e554e93bf0665831b220bc7
Source noteuspto-grants-2005_05