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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714111Generated: October 26, 2026

N-Methylbenzylamine → Benzyl-cyclohexylmethyl-methyl-amine

https://huagongshe.com/reaction/1714111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylbenzylamineHCID 7669—
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantCyclohexanecarboxaldehyde bisulfiteHCID 86612818—
Solvent1,1-DichloroethaneHCID 6365—
SolventEthyl AcetateHCID 8857—
ProductBenzyl-cyclohexylmethyl-methyl-amineHCID 12869919—

Reaction Steps

A suspension of cyclohexanecarboxaldehyde bisulfite adduct (5.0 mmol) and Et3N (5.5 mmol) in dichloroethane (20 mL) was stirred at room temperature for 15 min. The suspension was treated with N-methylbenzylamine (5.5 mmol) and was stirred for 45 min. NaBH(OAc)3 (7.0 mmol) was added portion-wise over approximately 30 min. After 16 h, the reaction mixture was diluted with EtOAc (80 mL), and was washed with 1 N NaOH (25 mL) followed by brine (25 mL). The organic layer was dried (MgSO4) and concentrated to yield benzyl-cyclohexylmethyl-methyl-amine as an oil. The crude material was purified by the General Purification Method as described above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795426B2
Source datasetuspto-grants-2010_09
ORD IDord-c48a5190a8f545a4a5f284472e82033f
Source noteuspto-grants-2010_09