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 | 101.9% |
Reaction Steps
To a stirred solution of 4-chloro-3-nitroaniline (51.8 g, 0.36 mol) in anhydrous DCM (300 mL) was added dropwise acetic anhydride (45 mL, 0.48 mol) at room temperature, and the resulting solution was stirred at room temperature for 3 h. The solvent was removed in vacuo, and Et2O was added to the residue. The precipitates were collected by filtration, washed thoroughly with Et2O, and dried under high vacuum to give 4′-chloro-3′-nitroacetanilide (78.7 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115640B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-74bef879f0de46b89e8eae68ef284cc5 |
| Source note | uspto-grants-2006_10 |