HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-4-methylaniline → 3-chloro-N-cyclohexylmethyl-4-methylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-4-methylaniline | HCID 7255 | — |
| Reactant | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-chloro-N-cyclohexylmethyl-4-methylaniline | HCID 22485162 | 85.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06890934B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-d70075e51e554e93bf0665831b220bc7 |
| Source note | uspto-grants-2005_05 |