HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[2-[2-Cyanophenoxy]phenyl]-4-hexyloxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzoyl chloride, 4-(hexyloxy)- | HCID 170235 | — |
| Reactant | 2-(2-Aminophenoxy)benzonitrile | HCID 20084388 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[2-[2-Cyanophenoxy]phenyl]-4-hexyloxybenzamide | HCID 20084541 | 77.3% |
Reaction Steps
In 20 ml of ether was dissolved 2.0 g of 2-(2-aminophenoxy)benzonitrile followed by addition of 2.04 g of triethylamine. Then, with ice-cooling and stirring, a solution of 2.67 g of 4-hexyloxybenzoyl chloride in 5 ml of ether was added dropwise. The mixture was further stirred at the same temperature for 1 hour. The reaction mixture was then washed with diluted hydrochloric acid and aqueous sodium hydrogen carbonate solution in that order, dried and concentrated. The residue was purified by silica gel column chromatography using ethyl acetate-n-hexane as the eluent and the relevant fraction was crystallized from diisopropyl ether to give 3.05 g of the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05399703 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-5b022dcb1f1d4d9ba8c88d9364ccec6c |
| Source note | uspto-grants-1995_03 |