HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitroaniline → N-(4-nitrophenyl)butanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-nitrophenyl)butanamide | HCID 346259 | 100% |
Reaction Steps
To a solution of 4-nitro aniline (1.01 g, 7.23 mmol) in anhydrous CH2Cl2 (20 mL) was added NMM (0.95 mL, 8.68 mmol). To the reaction mixture was added dropwise butyryl chloride (1.00 mL, 8.68 mmol) at 0° C. After stirring for 0.5 h, the reaction was extracted with CH2Cl2 (20 mL), washed with H2O (30 mL), dried over Na2SO4, and evaporated in vacuo to give N-(4-Nitrophenyl)butyramide (1.50 g, 100%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166744B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-b338941525c444359085adba3475575b |
| Source note | uspto-grants-2007_01 |