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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349353Generated: November 3, 2026

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

https://huagongshe.com/reaction/1349353

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 numberUS07211680B2
Source datasetuspto-grants-2007_05
ORD IDord-0d631c31c0fc404dabf8b781a9ef1f24
Source noteuspto-grants-2007_05