HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(4-Chlorophenoxy)aniline → 1-[4-(4-Chloro-phenoxy)-phenyl]-pyrrolidine-2,5-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(4-Chlorophenoxy)aniline | HCID 7578 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-[4-(4-Chloro-phenoxy)-phenyl]-pyrrolidine-2,5-dione | HCID 21834838 | 83% |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
A mixture of succinic anhydride (250 mg, 2.50 mmol) and 4-amino-4′-chloro diphenylether (500 mg, 2.27 mml) in toluene is heated to 110° C. for 14 h. and cooled down to room temperature. SOCl2 (1.5 mL) is added into the mixture and stirred at room temperature for 8 h. After the solvent is removed under vacuum, the residue is treated with saturated NaHCO3 aqueous solution (20 mL) and extracted with CHCl3 (3×50 mL). The combined organic layer is washed with brine and dried (MgSO4). After filtering the drying agent, the filtrate is concentrated and purified by flash column chromatography (silica gel, EtOAc/hexane 30%˜80%) to provide 1-[4-(4-chloro-phenoxy)-phenyl]-pyrrolidine-2,5-dione as white solid (570 mg, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431607B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-27372413f40c435287ff7bf4b98e13d5 |
| Source note | uspto-grants-2013_04 |