HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-tert-butyl-N-ethoxalyl-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | N-tert-Butyl-2-nitroaniline | HCID 10797892 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-tert-butyl-N-ethoxalyl-2-nitroaniline | HCID 20065638 | — |
Reaction Steps
To a stirred solution of 2-nitro-N-tert-butylaniline (37 g) and triethylamine (35 ml) in tetrahydrofuran (400 ml) was added dropwise a solution of ethoxalyl chloride (25 ml) in tetrahydrofuran (50 ml). The mixture was then brought to reflux temperature for 8 h. The solvent was removed by evaporation, and the residue was partitioned between ether (300 ml) and water (500 ml). The organic phase was washed twice with water, dried over Na2SO4 and evaporated. This left the title compound as light yellow crystals, m.p. 73°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04999353 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-231e8e5054254f97a84ddcc59e54f853 |
| Source note | uspto-grants-1991_03 |