HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylbutylamine → N-(2-nitrophenyl)-2-(N-n-butyl-N-methylamino)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylbutylamine | HCID 8068 | — |
| Reactant | 2-chloro-N-(2-nitrophenyl)acetamide | HCID 222443 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(2-nitrophenyl)-2-(N-n-butyl-N-methylamino)acetamide | HCID 21482991 | — |
Reaction Steps
N-(2-Nitrophenyl)-2-chloroacetamide (32.2 g) was dissolved in benzene (350 ml) and N-n-butylmethylamine (26.1 g) added. The mixture was boiled under reflux for 22 hours, the benzene evaporated off, and water (300 ml) added. The mixture was extracted with diethyl ether (3 × 200 ml), the extract dried with magnesium sulphate, filtered, and the ether evaporated off to give N-(2-nitrophenyl)-2-(N-n-butyl-N-methylamino)acetamide as a yellow oil which was used in the next stage without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005217 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-f245d71673294dfe91aed627a82039a0 |
| Source note | uspto-grants-1977_01 |