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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228169Generated: October 31, 2026

Triethylamine → N-cycloheptyl-N-methylamine

https://huagongshe.com/reaction/2228169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCycloheptanoneHCID 10400—
ReactantMethylamine hydrochlorideHCID 6364545—
Solvent1,2-DichloroethaneHCID 11—
ProductN-cycloheptyl-N-methylamineHCID 276275—

Reaction Steps

In 1,2-dichloroethane (50 ml) were suspended cycloheptanone (2 g), methylamine hydrochloride (3 g) and triethylamine (6.2 ml), and to the suspension was added sodium triacetoxy boron hydride (5.3 g) under ice-cooling. Under nitrogen atmosphere, the mixture was stirred at room temperature over night. The solvent was evaporated, and the residue was neutralized with sodium hydroxide. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution and dried with anhydrous magnesium sulfate. Under reduced pressure, the solvent was evaporated to give N-methylcycloheptylamine (1.8 g) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-51c4873a63b64d94be45c420348ee85d
Source noteuspto-grants-2002_07