HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-(7-Oxooctyl)isoindoline-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | N-[7-Oxo(6-carboethoxy)octyl]phthalimide | HCID 13801454 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-(7-Oxooctyl)isoindoline-1,3-dione | HCID 20511306 | — |
Reaction Steps
A mixture of 350 g of crude N-[7-oxo(6-carboethoxy)octyl]phthalimide and 1000 ml of acetic acid, concentrated hydrochloric acid, and water was refluxed for three hours. The reaction mixture was stripped, the residue dissolved in methylene chloride and basified with 2 N NaOH solution. The organic layer was separated, dried over anhydrous sodium sulfate, filtered and stripped to an orange oil, 73% pure by gc (SE-30, 90-280°@16°/min). This material was used without further purification in Preparation 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04370335 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-6f5c6ae26ff246d7a6a14057ba10a250 |
| Source note | uspto-grants-1983_01 |