Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577783Generated: October 28, 2026

Triethylamine → N-(Cyclopropylmethyl)cyclopropanecarboxamide

https://huagongshe.com/reaction/577783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclopropanecarboxylic acidHCID 15655—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantCyclopropanemethanamineHCID 75646—
ReactantHCID 178418300HCID 178418300—
SolventDichloromethaneHCID 6344—
ProductN-(Cyclopropylmethyl)cyclopropanecarboxamideHCID 2191606998.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyclopropyl carboxylic acid (1.0 g, 11.63 mmol) was added to a 50 mL two neck round bottom flask, along with DCM (25 mL). This mixture was cooled to 0° C., EDCI (4.15 g, 13.95 mmol) was added portionwise to the mixture with stirring under nitrogen atmosphere, and the temperature was maintained for 0.5 h. After this time, hydroxybenzotriazole (1.88 g, 13.95 mmol) was added to the 0° C. mixture which was stirred for 10 min, then triethylamine (1.7 g, 11.63 mmol) was added, and stirring of the mixture was continued at the same temperature for another 0.5 h. Then, cyclopropylmethylamine (0.825 g, 11.63 mmol) was added, and the reaction was allowed to reach RT, and stirring was continued overnight. The solvent was then removed in vacuo, and the crude residue was purified by passing through a column over 60-120 silica gel, eluting with dichloromethane, to afford the title compound (1.6 g), yield: 87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040558B2
Source datasetuspto-grants-2015_05
ORD IDord-a0e4a9eec1fa47deb6b014783dcaf890
Source noteuspto-grants-2015_05