HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-ethoxalyl-N-isopropyl-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | N-Isopropyl-2-nitroaniline | HCID 10583518 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-ethoxalyl-N-isopropyl-2-nitroaniline | HCID 14853709 | — |
Reaction Steps
To a stirred ice-cooled solution of 2-isopropylamino-nitrobenzene (19.5 g, 0.1 mole) and triethylamine (15 ml, 0.11 mole) in tetrahydrofurane (THF, 200 ml) was dropwise added ethoxalyl chloride. The ice bath was removed and the mixture was heated to reflux for 3 hours. The precipitated triethylammonium chloride was filtered off and the filtrate was evaporated in vacuo to give the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04999354 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-900bb01d1ba843eabfcc282d60563263 |
| Source note | uspto-grants-1991_03 |