HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromobenzene → 7-Chloro-3-hydroxy-3-phenyl-2-indolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | 7-Chloroisatin | HCID 344135 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 7-Chloro-3-hydroxy-3-phenyl-2-indolinone | HCID 21439427 | — |
Reaction Steps
A Grignard reagent prepared from 62 g. magnesium, 400 g. bromobenzene in two liters tetrahydrofuran (THF) is added to 181 g. (1.0 mole) 7-chloroisatin (1a) in two liters THF at a rate to keep a gentle reflux. After three hours of reflux, the reaction is cooled and decomposed with 350 ml. saturated ammonium chloride, filtered, and the THF stripped to give a dark oil. The oil is dissolved in aqueous sodium hydroxide and precipitated with hydrochloric acid. Recrystallization from aqueous ethanol gives 7-chloro-3-hydroxy-3-phenyl-2-indolinone, m.p. 154°-156°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04020179 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-98ca840e9e704ec283dd9b749a35a7e9 |
| Source note | uspto-grants-1977_04 |