HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Ethyl (acetyloxy)(4-chloro-3-nitrophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl (4-chloro-3-nitrophenyl)(hydroxy)acetate | HCID 86609828 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl (acetyloxy)(4-chloro-3-nitrophenyl)acetate | HCID 86609827 | — |
Reaction Steps
To a solution (6 mL) of the compound (1.46 g) prepared in Example 22 in pyridine, acetic anhydride (2 mL) was added, and the mixture was stirred for 1 hour at room temperature. The title compound (135 mg) having the following physical data was obtained by concentrating the reaction mixture and azeotroping in toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138335B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-555d4c3cd5e8463eb2a81316404c49a5 |
| Source note | uspto-grants-2012_03 |