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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478139Generated: November 1, 2026

Triethylamine → 1-bromo-N-(2-oxopentyl)-cyclopropane-1-carbamide

https://huagongshe.com/reaction/478139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-Aminopentan-2-one hydrochlorideHCID 12551761—
Reactant1-Bromocyclopropane-1-carboxylic acidHCID 12867480—
SolventDichloromethaneHCID 6344—
Product1-bromo-N-(2-oxopentyl)-cyclopropane-1-carbamideHCID 1800091570.9%

Reaction Steps

A mixture of 2.57 g of 1-bromocyclopropanecarboxylic acid 4 [H. M. R. Hoffmann et al. J. Org. Chem. 54, 6096 (1989)], 2.22 g of 1-amino-2-pentanone hydrochloride 5 [M. Jackman et al. J. Am. Chem. Soc. 70, 2884 (1948)] and 3.36 g of N,N′-dicyclohexylcarbodiimide in 234 ml of methylene chloride in the presence of 2.46 ml of triethylamine is stirred overnight at room temperature. Then, it is filtered, the filtrate is concentrated by evaporation, and the residue is chromatographed on silica gel with ethyl acetate/hexane. 2.74 g of 1-bromo-N-(2-oxopentyl)-cyclopropane-1-carbamide 6 is obtained as a crystallizing oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642218B2
Source datasetuspto-grants-2003_11
ORD IDord-20ed1aef6b504929a9e53964d84a2785
Source noteuspto-grants-2003_11