HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-bromo-N-(2-oxopentyl)-cyclopropane-1-carbamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Aminopentan-2-one hydrochloride | HCID 12551761 | — |
| Reactant | 1-Bromocyclopropane-1-carboxylic acid | HCID 12867480 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-bromo-N-(2-oxopentyl)-cyclopropane-1-carbamide | HCID 18000915 | 70.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06613920B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-1fab3457ae2f40fba59e070b2e1b8d01 |
| Source note | uspto-grants-2003_09 |