HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-(2-Ethoxyethyl)-2-nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-Chloro-2-nitrobenzene | HCID 6945 | — |
| Reactant | Ethoxyethylamine | HCID 66970 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2-Ethoxyethyl)-2-nitroaniline | HCID 13623317 | — |
Reaction Steps
According to the method of R. Iemura et al., J. Med. Chem., 29 1178-1183 (1986), combine 1-chloro-2-nitrobenzene (69.0 g, 440 mmol) and 2-aminoethyl ethyl ether (102.5 g, 1.15 mol) and heat to reflux. After 18 hours, cool and dilute the reaction mixture with ethyl acetate (400 mL). Extract with brine. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with dichloromethane to give N-(2-ethoxyethyl)-2-nitroaniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06194406B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-5a6ed0c5647449fdb89686f090e95aa3 |
| Source note | uspto-grants-2001_02 |