HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 5-Chloroisoindoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Propionic Acid | HCID 1032 | — |
| Reactant | 5-Chloro-2-tosylisoindoline | HCID 15167891 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Chloroisoindoline hydrochloride | HCID 49853502 | 97.2% |
Reaction Steps
1.0 g of 2-(p-toluensulphonyl)-5-chloroisoindoline and 1.0 g of phenol were added to a mixture of 8 ml of 48% hydrobromic acid and 1.4 ml of propionic acid, and then mixture was heated at reflux for 6 hours. The resultant reaction mixture was diluted with 10 ml of water and extracted twice with 50 ml of ethyl acetate. The water layer was basified with aqueous sodium hydroxide solution and extracted with ethyl acetate three times. The extract was concentrated and the crude product was diluted with 4N HCl/dioxane and stirred for 15 minutes before evaporating the HCl and then re-evaporating with toluene three times to give 0.3 g of 5-chloro-2,3-dihydro-1H-isoindole hydrochloride as a black solid. MS: [M+H]+ 153-15
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101648B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-30645b9ffc18409996e5585847d1b78f |
| Source note | uspto-grants-2012_01 |