HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381918Generated: November 2, 2026
Cyclohexylamine → 5-chloro-N-cyclohexylpentanamide
https://huagongshe.com/reaction/1381918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 5-Chlorovaleryl chloride | HCID 74089 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-chloro-N-cyclohexylpentanamide | HCID 11672974 | — |
Reaction Steps
A stirred solution of 5-chlorovaleryl chloride (50.0 g, 0.322 mol) in dichloromethane (300 ml) at 0° C. was treated dropwise with a solution containing cyclohexylamine (31.68 g, 0.320 mol), triethylamine (32.32 g, 0.320 mol) and dimethylaminopyridine (0.02 g) in dichloromethane (300 ml). The resulting solution was stirred for 2 hours at 0° C. and then for an additional 16 hours at room temperature. The solution was diluted with dichloromethane (400 ml), washed with water (3×200 ml), saturated aqueous sodium hydrogen carbonate (3×100 ml), saturated aqueous ammonium chloride (3×100 ml), and brine (2×100 ml) and then dried over anhydrous sodium sulfate. The solvent was evaporated off under reduced pressure to yield a crude product. The crude product was recrystallized from ethyl acetate-hexane to yield N-cyclohexyl-5-chloropentanamide as a colorless crystalline solid, having a melting point of 70°-71° C. and the following physical characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04804658 |
|---|
| Source dataset | uspto-grants-1989_02 |
|---|
| ORD ID | ord-a5fa354a8be8430e9d9400c4ef7a1c23 |
|---|
| Source note | uspto-grants-1989_02 |
|---|