HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-Chlorophthalic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Nitrophthalic anhydride | HCID 21631 | — |
| Reactant | Chlorophenyldichlorophosphine | HCID 12468898 | — |
| Solvent | Phenylphosphonic dichloride | HCID 69990 | — |
| Product | 3-Chlorophthalic anhydride | HCID 67014 | — |
Reaction Conditions
| Temperature | 170 °C |
|---|
Reaction Steps
Phenyltrichlorophosphonium hexachlorophosphide (4 g, 8.8 mM) was added to phenylphosphonic dichloride (10 ml). To this solutoin, 3 nitrophthalic anhydride (1.7 g, 8.8 mM) was added. The reaction mixture was heated to 170° C. for 12 hours, then cooled to room temperature and poured onto ice. After neutralizing with 50% aqueous sodium hydroxide, the reaction was extracted with ethyl acetate. The combined ethyl acetate extracts were washed with brine, dried over magnesium sulfate, and concentrated in vacuo to give 3-chlorophthalic anhydride (1.3 g, 81 wt. % yield) as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04814467 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-6f1afa0d9c8a4c72bb8eaf8c89314090 |
| Source note | uspto-grants-1989_03 |