HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitroaniline → p-Nitrophenylurethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | p-Nitrophenylurethane | HCID 230135 | — |
Reaction Steps
To a cooled (0° C.) suspension of 4-nitroaniline (10 g, 0.072 mol) and Et3N (10 mL) in CHCl3 (120 mL), was added dropwise ethyl chloroformate (6.9 mL) and the mixture was stirred under an argon atmosphere at room temperature overnight. CHCl3 was added and the resulting solution was washed with 1N HCl. The layers were separated, the aqueous phase was washed with CHCl3 and the combined organic extracts were dried and concentrated. The residue was chromatographed on silica gel (hexane:EtOAc, 30%) to afford N-(ethoxycarbonyl)-4-nitroaniline (1.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705504 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-0aa353dec71e421e93b481f6562f52de |
| Source note | uspto-grants-1998_01 |