HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(4-Chloro-3-nitrophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Chloro-3-nitroaniline | HCID 12477 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Chloro-3-nitrophenyl)acetamide | HCID 79672 | 96.5% |
Reaction Steps
To a stirred solution of 4-chloro-3-nitroaniline (17.3 g, 100 mmol) in DCM (150 mL) was added dropwise acetic anhydride (14 mL, 150 mmol) at ambient temperature. The mixture was stirred at ambient temperature for 2.5 h. The solvent was removed in vacuo, and Et2O was added to the residue. The precipitate was collected by filtration, washed with Et2O, and dried in vacuo to give N-(4-chloro-3-nitrophenyl)acetamide (20.7 g, 96%), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06696473B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-92b72ee7c9184a7282a64c27b1157a3c |
| Source note | uspto-grants-2004_02 |